FDA 510(k)

NEW ANTIMICRO. AGENTS:AUGMENTIN,AZTREONAM,CIPROFLO

K-Number: K874426 · 1987-12-02

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1987-12-02

Product CodeJWY

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

NEW ANTIMICRO. AGENTS:AUGMENTIN,AZTREONAM,CIPROFLO is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1987-12-02 under 510(k) number K874426. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW ANTIMICRO. AGENTS:AUGMENTIN,AZTREONAM,CIPROFLO?

NEW ANTIMICRO. AGENTS:AUGMENTIN,AZTREONAM,CIPROFLO is a medical device that received FDA 510(k) clearance on 1987-12-02. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K874426.

When did NEW ANTIMICRO. AGENTS:AUGMENTIN,AZTREONAM,CIPROFLO receive FDA 510(k) clearance?

NEW ANTIMICRO. AGENTS:AUGMENTIN,AZTREONAM,CIPROFLO received FDA 510(k) clearance on 1987-12-02, under 510(k) number K874426.

Who is the listed applicant for NEW ANTIMICRO. AGENTS:AUGMENTIN,AZTREONAM,CIPROFLO?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEW ANTIMICRO. AGENTS:AUGMENTIN,AZTREONAM,CIPROFLO?

The FDA product code for NEW ANTIMICRO. AGENTS:AUGMENTIN,AZTREONAM,CIPROFLO is JWY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic as applicant

K003062BACTEC MGIT 960 SIR KITS K0035530.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE K003461BD VACUTAINER PASSIVE SHIELDING BLOOD COLLECTION NEEDLE K002938B-D ULTRA-FINE III PEN NEEDLE; MODEL 31G X 3/16 K001364BD DIRECTIGEN FLU A+B K000762MOXIFLOXACIN, 5 UG, BBL SENSI-DISC

View all 632 devices →

Related Devices (Code: JWY)

K260447ETEST Gepotidacin (GEP) (0.016-256 µg/mL)bioMérieux SA K260696MTS Gepotidacin 0.016-256 µg/mLLiofilchem s.r.l.K252114MTS Aztreonam-Avibactam 0.016/4 - 256/4 µg/mLLiofilchem s.r.l.K252062The Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Colistin in the dilution range of 0.12-16 ug/mLThermo Fisher Scientific K250575The Sensititre 18 - 24 hour MIC or Breakpoint Susceptibility System with Aztreonam/avibactam in the dilution range of 0.008/4 - 64/4 ug/mLThermo Fisher Scientific K252014The Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Amikacin in the dilution range of 0.25-256 ug/mLThermo Fisher Scientific

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.