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FDA 510(k)

MUELLER HINTON AGAR W/HEMOGLOBIN

K-Number: K760459 · 1976-09-03

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1976-09-03
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MUELLER HINTON AGAR W/HEMOGLOBIN 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 1976-09-03 under 510(k) number K760459. 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 MUELLER HINTON AGAR W/HEMOGLOBIN?

MUELLER HINTON AGAR W/HEMOGLOBIN is a medical device that received FDA 510(k) clearance on 1976-09-03. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K760459.

When did MUELLER HINTON AGAR W/HEMOGLOBIN receive FDA 510(k) clearance?

MUELLER HINTON AGAR W/HEMOGLOBIN received FDA 510(k) clearance on 1976-09-03, under 510(k) number K760459.

Who is the listed applicant for MUELLER HINTON AGAR W/HEMOGLOBIN?

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 MUELLER HINTON AGAR W/HEMOGLOBIN?

The FDA product code for MUELLER HINTON AGAR W/HEMOGLOBIN is JSG.

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Related Devices (Code: 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.

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