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FDA 510(k)

ANAEROBIC BLOOD AGAR

K-Number: K812795 · 1981-10-20

Decision Date1981-10-20
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANAEROBIC BLOOD AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Isle Media and Sterile Products, Inc.. It received FDA 510(k) clearance on 1981-10-20 under 510(k) number K812795. 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 ANAEROBIC BLOOD AGAR?

ANAEROBIC BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1981-10-20. The listed applicant is Isle Media and Sterile Products, Inc.. The 510(k) number is K812795.

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

ANAEROBIC BLOOD AGAR received FDA 510(k) clearance on 1981-10-20, under 510(k) number K812795.

Who is the listed applicant for ANAEROBIC BLOOD AGAR?

The FDA 510(k) record lists Isle Media and Sterile Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANAEROBIC BLOOD AGAR?

The FDA product code for ANAEROBIC BLOOD AGAR is JSG.

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 Isle Media and Sterile Products, Inc. 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 93 devices →

Related Devices (Code: JSG)

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

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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