LOMBARD-DOWELL BROTH MEDIUM W/LACTATE
K-Number: K790624 · 1979-04-23
Advertisement
Device Summary
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.
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.
Advertisement