MUELLER HINTON AGAR
K-Number: K850715 · 1985-03-22
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON AGAR?
MUELLER HINTON AGAR is a medical device that received FDA 510(k) clearance on 1985-03-22. The listed applicant is Rapid City Regional Hospital, Inc.. The 510(k) number is K850715.
When did MUELLER HINTON AGAR receive FDA 510(k) clearance?
MUELLER HINTON AGAR received FDA 510(k) clearance on 1985-03-22, under 510(k) number K850715.
Who is the listed applicant for MUELLER HINTON AGAR?
The FDA 510(k) record lists Rapid City Regional Hospital, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON AGAR?
The FDA product code for MUELLER HINTON AGAR 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 Rapid City Regional Hospital, 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: 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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