VCAT ANTIBIOTIC SUPPLEMENT
K-Number: K822459 · 1982-09-14
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Device Summary
Frequently Asked Questions
What is the VCAT ANTIBIOTIC SUPPLEMENT?
VCAT ANTIBIOTIC SUPPLEMENT is a medical device that received FDA 510(k) clearance on 1982-09-14. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K822459.
When did VCAT ANTIBIOTIC SUPPLEMENT receive FDA 510(k) clearance?
VCAT ANTIBIOTIC SUPPLEMENT received FDA 510(k) clearance on 1982-09-14, under 510(k) number K822459.
Who is the listed applicant for VCAT ANTIBIOTIC SUPPLEMENT?
The FDA 510(k) record lists Oxoid U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VCAT ANTIBIOTIC SUPPLEMENT?
The FDA product code for VCAT ANTIBIOTIC SUPPLEMENT is JSK.
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 Oxoid U.S.A., 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: JSK)
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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