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FDA 510(k)

ANAEROBE BLOOD AGAR

K-Number: K802397 · 1980-10-23

ApplicantGranite Diagnostics, Inc.
Decision Date1980-10-23
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANAEROBE BLOOD AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Granite Diagnostics, Inc.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K802397. 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 ANAEROBE BLOOD AGAR?

ANAEROBE BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K802397.

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

ANAEROBE BLOOD AGAR received FDA 510(k) clearance on 1980-10-23, under 510(k) number K802397.

Who is the listed applicant for ANAEROBE BLOOD AGAR?

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

What is the FDA product code for ANAEROBE BLOOD AGAR?

The FDA product code for ANAEROBE BLOOD AGAR is JSG.

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Other records listing Granite Diagnostics, 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.

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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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