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FDA 510(k)

CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS

K-Number: K893754 · 1989-07-14

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1989-07-14
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS 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 1989-07-14 under 510(k) number K893754. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS?

CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K893754.

When did CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS receive FDA 510(k) clearance?

CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893754.

Who is the listed applicant for CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS?

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 CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS?

The FDA product code for CEFIXIME, 5 MCG SENSI-DISC ANTIMIC SUSCEP TEST DIS is JTN.

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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.

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