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FDA 510(k)

COLUMBIA BLOOD AGAR WITH 5% SHEEP BLOOD

K-Number: K864240 · 1987-03-31

Decision Date1987-03-31
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

COLUMBIA BLOOD AGAR WITH 5% SHEEP BLOOD is the device name listed in this FDA 510(k) record. The listed applicant is Mds Laboratories, Inc.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K864240. 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 COLUMBIA BLOOD AGAR WITH 5% SHEEP BLOOD?

COLUMBIA BLOOD AGAR WITH 5% SHEEP BLOOD is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Mds Laboratories, Inc.. The 510(k) number is K864240.

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

COLUMBIA BLOOD AGAR WITH 5% SHEEP BLOOD received FDA 510(k) clearance on 1987-03-31, under 510(k) number K864240.

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

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

What is the FDA product code for COLUMBIA BLOOD AGAR WITH 5% SHEEP BLOOD?

The FDA product code for COLUMBIA BLOOD AGAR WITH 5% SHEEP BLOOD 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 Mds Laboratories, 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 21 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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