VOTEL-JOHNSON AGAR (MODIFIED)
K-Number: K810933 · 1981-04-14
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Device Summary
Frequently Asked Questions
What is the VOTEL-JOHNSON AGAR (MODIFIED)?
VOTEL-JOHNSON 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 K810933.
When did VOTEL-JOHNSON AGAR (MODIFIED) receive FDA 510(k) clearance?
VOTEL-JOHNSON AGAR (MODIFIED) received FDA 510(k) clearance on 1981-04-14, under 510(k) number K810933.
Who is the listed applicant for VOTEL-JOHNSON 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 VOTEL-JOHNSON AGAR (MODIFIED)?
The FDA product code for VOTEL-JOHNSON 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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