PATIENTMATE TM
K-Number: K854754 · 1986-02-04
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Device Summary
Frequently Asked Questions
What is the PATIENTMATE TM?
PATIENTMATE TM is a medical device that received FDA 510(k) clearance on 1986-02-04. The listed applicant is Trend Medical, Inc.. The 510(k) number is K854754.
When did PATIENTMATE TM receive FDA 510(k) clearance?
PATIENTMATE TM received FDA 510(k) clearance on 1986-02-04, under 510(k) number K854754.
Who is the listed applicant for PATIENTMATE TM?
The FDA 510(k) record lists Trend Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENTMATE TM?
The FDA product code for PATIENTMATE TM is FPA.
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 Trend Medical, 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: FPA)
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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