FDA 510(k)

PEPTONE YEAST EXTRACT GLUCOSE BROTH

K-Number: K803026 · 1980-12-22

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1980-12-22

Product CodeJSC

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

PEPTONE YEAST EXTRACT GLUCOSE BROTH 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 1980-12-22 under 510(k) number K803026. The device is classified under product code JSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEPTONE YEAST EXTRACT GLUCOSE BROTH?

PEPTONE YEAST EXTRACT GLUCOSE BROTH is a medical device that received FDA 510(k) clearance on 1980-12-22. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K803026.

When did PEPTONE YEAST EXTRACT GLUCOSE BROTH receive FDA 510(k) clearance?

PEPTONE YEAST EXTRACT GLUCOSE BROTH received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803026.

Who is the listed applicant for PEPTONE YEAST EXTRACT GLUCOSE BROTH?

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 PEPTONE YEAST EXTRACT GLUCOSE BROTH?

The FDA product code for PEPTONE YEAST EXTRACT GLUCOSE BROTH is JSC.

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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.