FDA 510(k)

NEOMYCIN AGAR WITH 5% SHEEP BLOOD

K-Number: K761359 · 1977-01-14

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1977-01-14

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

NEOMYCIN AGAR WITH 5% SHEEP BLOOD 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 1977-01-14 under 510(k) number K761359. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOMYCIN AGAR WITH 5% SHEEP BLOOD?

NEOMYCIN AGAR WITH 5% SHEEP BLOOD is a medical device that received FDA 510(k) clearance on 1977-01-14. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K761359.

When did NEOMYCIN AGAR WITH 5% SHEEP BLOOD receive FDA 510(k) clearance?

NEOMYCIN AGAR WITH 5% SHEEP BLOOD received FDA 510(k) clearance on 1977-01-14, under 510(k) number K761359.

Who is the listed applicant for NEOMYCIN AGAR WITH 5% SHEEP BLOOD?

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 NEOMYCIN AGAR WITH 5% SHEEP BLOOD?

The FDA product code for NEOMYCIN AGAR WITH 5% SHEEP BLOOD is JSJ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.