MUELLER HINTON AGAR WITH 2% NACI
K-Number: K960313 · 1996-03-25
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON AGAR WITH 2% NACI?
MUELLER HINTON AGAR WITH 2% NACI is a medical device that received FDA 510(k) clearance on 1996-03-25. The listed applicant is Remel, L.P.. The 510(k) number is K960313.
When did MUELLER HINTON AGAR WITH 2% NACI receive FDA 510(k) clearance?
MUELLER HINTON AGAR WITH 2% NACI received FDA 510(k) clearance on 1996-03-25, under 510(k) number K960313.
Who is the listed applicant for MUELLER HINTON AGAR WITH 2% NACI?
The FDA 510(k) record lists Remel, L.P. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON AGAR WITH 2% NACI?
The FDA product code for MUELLER HINTON AGAR WITH 2% NACI is JTZ.
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 Remel, L.P. 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: JTZ)
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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