MOBILE SOPHIE MODIFICATION— 510(k) K934373

Substantially Equivalent

Planmed OY

FDA 510(k) clearance K934373 for MOBILE SOPHIE MODIFICATION, Substantially Equivalent on 1994-04-07. Applicant: Planmed OY.

Clearance details

Applicant: Planmed OY
Product code: Code IZH
Advisory panel: Radiology
Date received: 1993-09-08
Decision date: 1994-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Helsinki, FI

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