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FDA 510(k)

MUCATE AGAR, SLANTS AND MUCATE BROTH

K-Number: K872020 · 1987-06-02

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1987-06-02
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MUCATE AGAR, SLANTS AND MUCATE 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 1987-06-02 under 510(k) number K872020. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUCATE AGAR, SLANTS AND MUCATE BROTH?

MUCATE AGAR, SLANTS AND MUCATE BROTH is a medical device that received FDA 510(k) clearance on 1987-06-02. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K872020.

When did MUCATE AGAR, SLANTS AND MUCATE BROTH receive FDA 510(k) clearance?

MUCATE AGAR, SLANTS AND MUCATE BROTH received FDA 510(k) clearance on 1987-06-02, under 510(k) number K872020.

Who is the listed applicant for MUCATE AGAR, SLANTS AND MUCATE 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 MUCATE AGAR, SLANTS AND MUCATE BROTH?

The FDA product code for MUCATE AGAR, SLANTS AND MUCATE BROTH is JSH.

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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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