MUELLER HINTON AGAR - SUPPLEMENTED
K-Number: K864248 · 1987-03-31
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON AGAR - SUPPLEMENTED?
MUELLER HINTON AGAR - SUPPLEMENTED is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Mds Laboratories, Inc.. The 510(k) number is K864248.
When did MUELLER HINTON AGAR - SUPPLEMENTED receive FDA 510(k) clearance?
MUELLER HINTON AGAR - SUPPLEMENTED received FDA 510(k) clearance on 1987-03-31, under 510(k) number K864248.
Who is the listed applicant for MUELLER HINTON AGAR - SUPPLEMENTED?
The FDA 510(k) record lists Mds Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON AGAR - SUPPLEMENTED?
The FDA product code for MUELLER HINTON AGAR - SUPPLEMENTED 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 Mds Laboratories, 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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