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FDA 510(k)

CHOPPED MEAT GLUCOSE MEDIUM

K-Number: K790621 · 1979-04-23

Decision Date1979-04-23
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CHOPPED MEAT GLUCOSE MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Anaerobe Systems. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790621. 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 CHOPPED MEAT GLUCOSE MEDIUM?

CHOPPED MEAT GLUCOSE MEDIUM is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Anaerobe Systems. The 510(k) number is K790621.

When did CHOPPED MEAT GLUCOSE MEDIUM receive FDA 510(k) clearance?

CHOPPED MEAT GLUCOSE MEDIUM received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790621.

Who is the listed applicant for CHOPPED MEAT GLUCOSE MEDIUM?

The FDA 510(k) record lists Anaerobe Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHOPPED MEAT GLUCOSE MEDIUM?

The FDA product code for CHOPPED MEAT GLUCOSE MEDIUM 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 Anaerobe Systems 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 52 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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