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FDA 510(k)

LOMBARD DOWELL BROTH MEDIUMW/TH REONINE

K-Number: K790620 · 1979-04-23

ApplicantAnaerobe Systems
Decision Date1979-04-23
Product CodeJSC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

LOMBARD DOWELL BROTH MEDIUMW/TH REONINE 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 K790620. The device is classified under product code JSC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOMBARD DOWELL BROTH MEDIUMW/TH REONINE?

LOMBARD DOWELL BROTH MEDIUMW/TH REONINE 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 K790620.

When did LOMBARD DOWELL BROTH MEDIUMW/TH REONINE receive FDA 510(k) clearance?

LOMBARD DOWELL BROTH MEDIUMW/TH REONINE received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790620.

Who is the listed applicant for LOMBARD DOWELL BROTH MEDIUMW/TH REONINE?

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 LOMBARD DOWELL BROTH MEDIUMW/TH REONINE?

The FDA product code for LOMBARD DOWELL BROTH MEDIUMW/TH REONINE is JSC.

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Related Devices (Code: JSC)

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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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