AUTOCUFF (PHOTOS ENCLOSED WITH 510K
K-Number: K822286 · 1982-08-27
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Device Summary
Frequently Asked Questions
What is the AUTOCUFF (PHOTOS ENCLOSED WITH 510K?
AUTOCUFF (PHOTOS ENCLOSED WITH 510K is a medical device that received FDA 510(k) clearance on 1982-08-27. The listed applicant is Partamed, Inc.. The 510(k) number is K822286.
When did AUTOCUFF (PHOTOS ENCLOSED WITH 510K receive FDA 510(k) clearance?
AUTOCUFF (PHOTOS ENCLOSED WITH 510K received FDA 510(k) clearance on 1982-08-27, under 510(k) number K822286.
Who is the listed applicant for AUTOCUFF (PHOTOS ENCLOSED WITH 510K?
The FDA 510(k) record lists Partamed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTOCUFF (PHOTOS ENCLOSED WITH 510K?
The FDA product code for AUTOCUFF (PHOTOS ENCLOSED WITH 510K is KZD.
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.
Related Devices (Code: KZD)
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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