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FDA 510(k)

COLUMBIA AGAR WITH5% SHEEP

K-Number: K791622 · 1979-09-24

ApplicantAmerican Laboratory Supply, Inc.
Decision Date1979-09-24
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

COLUMBIA AGAR WITH5% SHEEP is the device name listed in this FDA 510(k) record. The listed applicant is American Laboratory Supply, Inc.. It received FDA 510(k) clearance on 1979-09-24 under 510(k) number K791622. 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 AGAR WITH5% SHEEP?

COLUMBIA AGAR WITH5% SHEEP is a medical device that received FDA 510(k) clearance on 1979-09-24. The listed applicant is American Laboratory Supply, Inc.. The 510(k) number is K791622.

When did COLUMBIA AGAR WITH5% SHEEP receive FDA 510(k) clearance?

COLUMBIA AGAR WITH5% SHEEP received FDA 510(k) clearance on 1979-09-24, under 510(k) number K791622.

Who is the listed applicant for COLUMBIA AGAR WITH5% SHEEP?

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

What is the FDA product code for COLUMBIA AGAR WITH5% SHEEP?

The FDA product code for COLUMBIA AGAR WITH5% SHEEP is JSG.

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Other records listing American Laboratory Supply, Inc. as applicant

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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.

K882495THIOGLYCOLLATE BROTH W/VITA. K & HEMIN - #T3007Lakewood Biochemical Co., Inc.K881558TRYPTOSE AGARAcumedia Manufacturers, Inc.K881550OF BASAL MEDIUMAcumedia Manufacturers, Inc.K881557TRYPTONEAcumedia Manufacturers, Inc.K881564TRYPTOSE BLOOD AGAR BASE W/YEAST EXTRACTAcumedia Manufacturers, Inc.K881533BLOOD AGAR BASE NO. 2Acumedia Manufacturers, Inc.

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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