Cruxi research & evidence
FDA 510(k) Submission Services evidence guides — page 23
Compare documented facts, dated analyses and evidence that can change your project scope. Confirm applicability with a specialist.
Compare FDA 510(k) Submission Services providers- Arterial Pressure Monitoring Set/Tray (K180846): indications, design and recorded evidenceRegulatory decision evidence
- Arterial Pressure Monitoring Set/Tray (K254278): indications, design and recorded evidenceRegulatory decision evidence
- Arterial Pressure Monitoring Set/Tray (K261455): indications, design and recorded evidenceRegulatory decision evidence
- ArtiFascia (K223445): indications, design and recorded evidenceRegulatory decision evidence
- Artimes pro Balloon Dilatation Catheter (K203390): indications, design and recorded evidenceRegulatory decision evidence
- Ascend VBR System, Ascend NanoTec VBR System (K232173): indications, design and recorded evidenceRegulatory decision evidence
- Ascent3T Neonatal Magnetic Resonance Imaging System (K253499): indications, design and recorded evidenceRegulatory decision evidence
- Aspiron(TM) Aspiration Catheter (K190619): indications, design and recorded evidenceRegulatory decision evidence
- Assay To Measure Pct To Aid In The Risk Assessment Of Critically Ill Patients On Their First Day Of Icu Admission (PTF) — FDA decisions, comparisons and evidenceFDA record research
- Assay, 1,5-Anhydroglucitol (15ag) (NOZ) — FDA decisions, comparisons and evidenceFDA record research
- Assay, Direct, Nucleic Acid Amplification, Q Fever (OVF) — FDA decisions, comparisons and evidenceFDA record research
- Assay, Nucleic Acid Amplification, Bacillus Anthracis (NHT) — FDA decisions, comparisons and evidenceFDA record research
- Assay, Proliferation, In Vitro, T Lymphocyte (NID) — FDA decisions, comparisons and evidenceFDA record research
- Assert-IQ (DM5000); Assert-IQ (DM5300); Assert-IQ (DM5500); Merlin.net (MN7000) (K251221): indications, design and recorded evidenceRegulatory decision evidence
- AssureTech Panel Dip Tests, AssureTech Quick Cup Tests (K181768): indications, design and recorded evidenceRegulatory decision evidence
- AssureTech Panel Dip Tests; AssureTech Quick Cup Tests; AssureTech Multi-drug Urine Test Panel; AssureTech Multi-drug Urine Test Cup (K243996): indications, design and recorded evidenceRegulatory decision evidence
- AssureTech Quick Cup Tests;AssureTech Multi-drug Urine Test Cup (K261984): indications, design and recorded evidenceRegulatory decision evidence
- Assut Filbloc Permanent Sutures (K171039): indications, design and recorded evidenceRegulatory decision evidence
- Atalante (K221859): indications, design and recorded evidenceRegulatory decision evidence
- Atalante X (K232077): indications, design and recorded evidenceRegulatory decision evidence
- Atellica IM Ferritin Assay (K171642): indications, design and recorded evidenceRegulatory decision evidence
- Atellica Solution, Atellica A-LYTE Integrated Multisensor Na+/K+/CI-, Atellica CH Albumin BCP Reagent (Alb_p), Atellica IM Thyroid Stimulating Hormone TSH, Atellica CH Vancomycin (Vanc) (K161954): indications, design and recorded evidenceRegulatory decision evidence
- Athena III Cervical Plate System (K230301): indications, design and recorded evidenceRegulatory decision evidence
- Atlas Percussion Adjusting Instrument (K172536): indications, design and recorded evidenceRegulatory decision evidence
- Atlas SPEEDER Head/Neck (K142802): indications, design and recorded evidenceRegulatory decision evidence
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