#19041-150X15MM MUELLER HINTON
K-Number: K820792 · 1982-04-08
Advertisement
Device Summary
Frequently Asked Questions
What is the #19041-150X15MM MUELLER HINTON?
#19041-150X15MM MUELLER HINTON is a medical device that received FDA 510(k) clearance on 1982-04-08. The listed applicant is Biomedica, Inc.. The 510(k) number is K820792.
When did #19041-150X15MM MUELLER HINTON receive FDA 510(k) clearance?
#19041-150X15MM MUELLER HINTON received FDA 510(k) clearance on 1982-04-08, under 510(k) number K820792.
Who is the listed applicant for #19041-150X15MM MUELLER HINTON?
The FDA 510(k) record lists Biomedica, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for #19041-150X15MM MUELLER HINTON?
The FDA product code for #19041-150X15MM MUELLER HINTON 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 Biomedica, 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.
Advertisement