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FDA 510(k)

CEFUROXIME 30 MCG SENSI-DISC

K-Number: K832515 · 1983-10-14

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1983-10-14
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CEFUROXIME 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 1983-10-14 under 510(k) number K832515. 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 CEFUROXIME 30 MCG SENSI-DISC?

CEFUROXIME 30 MCG SENSI-DISC is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K832515.

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

CEFUROXIME 30 MCG SENSI-DISC received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832515.

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

The FDA product code for CEFUROXIME 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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