PERFRINGENS SUPPLEMENT B
K-Number: K800263 · 1980-03-12
Advertisement
Device Summary
Frequently Asked Questions
What is the PERFRINGENS SUPPLEMENT B?
PERFRINGENS SUPPLEMENT B is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K800263.
When did PERFRINGENS SUPPLEMENT B receive FDA 510(k) clearance?
PERFRINGENS SUPPLEMENT B received FDA 510(k) clearance on 1980-03-12, under 510(k) number K800263.
Who is the listed applicant for PERFRINGENS SUPPLEMENT B?
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 PERFRINGENS SUPPLEMENT B?
The FDA product code for PERFRINGENS SUPPLEMENT B 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.
Advertisement