SS AGAR (MODIFIED)
K-Number: K810931 · 1981-04-14
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Device Summary
Frequently Asked Questions
What is the SS AGAR (MODIFIED)?
SS AGAR (MODIFIED) is a medical device that received FDA 510(k) clearance on 1981-04-14. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K810931.
When did SS AGAR (MODIFIED) receive FDA 510(k) clearance?
SS AGAR (MODIFIED) received FDA 510(k) clearance on 1981-04-14, under 510(k) number K810931.
Who is the listed applicant for SS AGAR (MODIFIED)?
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 SS AGAR (MODIFIED)?
The FDA product code for SS AGAR (MODIFIED) 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 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: 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.
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