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FDA 510(k)

CDC ANAEROBE BLOOD AGAR PLATE

K-Number: K834418 · 1984-01-17

Decision Date1984-01-17
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CDC ANAEROBE BLOOD AGAR PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Otisville Biotech, Inc.. It received FDA 510(k) clearance on 1984-01-17 under 510(k) number K834418. 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 CDC ANAEROBE BLOOD AGAR PLATE?

CDC ANAEROBE BLOOD AGAR PLATE is a medical device that received FDA 510(k) clearance on 1984-01-17. The listed applicant is Otisville Biotech, Inc.. The 510(k) number is K834418.

When did CDC ANAEROBE BLOOD AGAR PLATE receive FDA 510(k) clearance?

CDC ANAEROBE BLOOD AGAR PLATE received FDA 510(k) clearance on 1984-01-17, under 510(k) number K834418.

Who is the listed applicant for CDC ANAEROBE BLOOD AGAR PLATE?

The FDA 510(k) record lists Otisville Biotech, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CDC ANAEROBE BLOOD AGAR PLATE?

The FDA product code for CDC ANAEROBE BLOOD AGAR PLATE 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 Otisville Biotech, 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 98 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

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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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