ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCO
K-Number: K820555 · 1982-03-16
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Device Summary
Frequently Asked Questions
What is the ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCO?
ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCO is a medical device that received FDA 510(k) clearance on 1982-03-16. The listed applicant is American Laboratory Supply, Inc.. The 510(k) number is K820555.
When did ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCO receive FDA 510(k) clearance?
ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCO received FDA 510(k) clearance on 1982-03-16, under 510(k) number K820555.
Who is the listed applicant for ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCO?
The FDA 510(k) record lists American Laboratory Supply, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCO?
The FDA product code for ANAEROBE BLOOD AGAR W/KANAMYCIN & VANCO is JSJ.
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 American Laboratory Supply, 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.
Related Devices (Code: JSJ)
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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