MUELLER HINTON AGAR WITH THYMIDINE
K-Number: K780959 · 1978-10-24
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Device Summary
Frequently Asked Questions
What is the MUELLER HINTON AGAR WITH THYMIDINE?
MUELLER HINTON AGAR WITH THYMIDINE is a medical device that received FDA 510(k) clearance on 1978-10-24. The listed applicant is Pittsburgh Micro-Media, Inc.. The 510(k) number is K780959.
When did MUELLER HINTON AGAR WITH THYMIDINE receive FDA 510(k) clearance?
MUELLER HINTON AGAR WITH THYMIDINE received FDA 510(k) clearance on 1978-10-24, under 510(k) number K780959.
Who is the listed applicant for MUELLER HINTON AGAR WITH THYMIDINE?
The FDA 510(k) record lists Pittsburgh Micro-Media, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MUELLER HINTON AGAR WITH THYMIDINE?
The FDA product code for MUELLER HINTON AGAR WITH THYMIDINE 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 Pittsburgh Micro-Media, 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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