MUELLER HINTON AGAR W/OXACILLIN
K-Number: K941985 · 1994-08-24
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON AGAR W/OXACILLIN?
MUELLER HINTON AGAR W/OXACILLIN is a medical device that received FDA 510(k) clearance on 1994-08-24. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. The 510(k) number is K941985.
When did MUELLER HINTON AGAR W/OXACILLIN receive FDA 510(k) clearance?
MUELLER HINTON AGAR W/OXACILLIN received FDA 510(k) clearance on 1994-08-24, under 510(k) number K941985.
Who is the listed applicant for MUELLER HINTON AGAR W/OXACILLIN?
The FDA 510(k) record lists Carr-Scarborough Microbiologicals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON AGAR W/OXACILLIN?
The FDA product code for MUELLER HINTON AGAR W/OXACILLIN 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 Carr-Scarborough Microbiologicals, 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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