Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LOMBARD-DOWELL BROTH MEDIUM W/LACTATE

K-Number: K790624 · 1979-04-23

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

Device Summary

LOMBARD-DOWELL BROTH MEDIUM W/LACTATE 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 K790624. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOMBARD-DOWELL BROTH MEDIUM W/LACTATE?

LOMBARD-DOWELL BROTH MEDIUM W/LACTATE 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 K790624.

When did LOMBARD-DOWELL BROTH MEDIUM W/LACTATE receive FDA 510(k) clearance?

LOMBARD-DOWELL BROTH MEDIUM W/LACTATE received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790624.

Who is the listed applicant for LOMBARD-DOWELL BROTH MEDIUM W/LACTATE?

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 MEDIUM W/LACTATE?

The FDA product code for LOMBARD-DOWELL BROTH MEDIUM W/LACTATE is JSI.

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: JSI)

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.

↑