POLYSCAN DIGITAL SCANNER— 510(k) K944684

Name: FDA 510(k) clearance K944684
Creator: U.S. Food and Drug Administration
Published: 1995-05-15

Substantially Equivalent

Mse Medizintechnik GmbH & Co. KG

FDA 510(k) clearance K944684 for POLYSCAN DIGITAL SCANNER, Substantially Equivalent on 1995-05-15. Applicant: Mse Medizintechnik GmbH & Co. KG. Device class: 1.

Clearance details

Applicant: Mse Medizintechnik GmbH & Co. KG
Product code: Code IYW
Device class: Class 1
Regulation: 21 CFR 892.1300
Advisory panel: Radiology
Date received: 1994-09-22
Decision date: 1995-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rodemark, DE

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