FDA 510(k)

ENRICHED THIOGLYCOLLATE MEDIUM

K-Number: K803023 · 1980-12-22

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1980-12-22

Product CodeJSG

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

ENRICHED THIOGLYCOLLATE MEDIUM 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 K803023. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENRICHED THIOGLYCOLLATE MEDIUM?

ENRICHED THIOGLYCOLLATE MEDIUM 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 K803023.

When did ENRICHED THIOGLYCOLLATE MEDIUM receive FDA 510(k) clearance?

ENRICHED THIOGLYCOLLATE MEDIUM received FDA 510(k) clearance on 1980-12-22, under 510(k) number K803023.

Who is the listed applicant for ENRICHED THIOGLYCOLLATE MEDIUM?

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 ENRICHED THIOGLYCOLLATE MEDIUM?

The FDA product code for ENRICHED THIOGLYCOLLATE MEDIUM is JSG.

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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.