VERIMED MYO/PREMS
K-Number: K874212 · 1988-08-08
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Device Summary
Frequently Asked Questions
What is the VERIMED MYO/PREMS?
VERIMED MYO/PREMS is a medical device that received FDA 510(k) clearance on 1988-08-08. The listed applicant is Verimed Holdings, Inc.. The 510(k) number is K874212.
When did VERIMED MYO/PREMS receive FDA 510(k) clearance?
VERIMED MYO/PREMS received FDA 510(k) clearance on 1988-08-08, under 510(k) number K874212.
Who is the listed applicant for VERIMED MYO/PREMS?
The FDA 510(k) record lists Verimed Holdings, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERIMED MYO/PREMS?
The FDA product code for VERIMED MYO/PREMS is IPF.
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 Verimed Holdings, 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: IPF)
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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