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FDA 510(k)

CEFOTAXIME 30 MCG. SENSI-DISC.

K-Number: K810564 · 1981-03-31

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1981-03-31
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CEFOTAXIME 30 MCG. SENSI-DISC. 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 1981-03-31 under 510(k) number K810564. 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 CEFOTAXIME 30 MCG. SENSI-DISC.?

CEFOTAXIME 30 MCG. SENSI-DISC. is a medical device that received FDA 510(k) clearance on 1981-03-31. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K810564.

When did CEFOTAXIME 30 MCG. SENSI-DISC. receive FDA 510(k) clearance?

CEFOTAXIME 30 MCG. SENSI-DISC. received FDA 510(k) clearance on 1981-03-31, under 510(k) number K810564.

Who is the listed applicant for CEFOTAXIME 30 MCG. SENSI-DISC.?

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 CEFOTAXIME 30 MCG. SENSI-DISC.?

The FDA product code for CEFOTAXIME 30 MCG. SENSI-DISC. 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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