PRESS 1 PRESS 2 9220 UPDATING OF THE MODULE— 510(k) K912816

Name: FDA 510(k) clearance K912816
Creator: U.S. Food and Drug Administration
Published: 1992-04-10

Substantially Equivalent

S & W Medico Teknik

FDA 510(k) clearance K912816 for PRESS 1 PRESS 2 9220 UPDATING OF THE MODULE, Substantially Equivalent on 1992-04-10. Applicant: S & W Medico Teknik. Device class: 2.

Clearance details

Applicant: S & W Medico Teknik
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1991-06-18
Decision date: 1992-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denmark, DK

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