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FDA 510(k)

FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT

K-Number: K792056 · 1979-11-16

Decision Date1979-11-16
Product CodeJSC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1979-11-16 under 510(k) number K792056. The device is classified under product code JSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT?

FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K792056.

When did FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT receive FDA 510(k) clearance?

FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT received FDA 510(k) clearance on 1979-11-16, under 510(k) number K792056.

Who is the listed applicant for FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT?

The FDA product code for FISHER DIAGNOSTICS ANAEROBIC BLOOD CULT is JSC.

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 Fisher Scientific Co., LLC 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 89 devices →

Related Devices (Code: JSC)

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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