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FDA 510(k)

NEOMYCIN BLOOD AGAR

K-Number: K843492 · 1984-10-02

Decision Date1984-10-02
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

NEOMYCIN BLOOD AGAR 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 1984-10-02 under 510(k) number K843492. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOMYCIN BLOOD AGAR?

NEOMYCIN BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1984-10-02. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K843492.

When did NEOMYCIN BLOOD AGAR receive FDA 510(k) clearance?

NEOMYCIN BLOOD AGAR received FDA 510(k) clearance on 1984-10-02, under 510(k) number K843492.

Who is the listed applicant for NEOMYCIN BLOOD AGAR?

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 BLOOD AGAR?

The FDA product code for NEOMYCIN BLOOD AGAR is JSI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 632 devices →

Related Devices (Code: JSI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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