DIGISCAN 2— 510(k) K924459

Substantially Equivalent

Siemens Medical Solutions USA, Inc.

FDA 510(k) clearance K924459 for DIGISCAN 2, Substantially Equivalent on 1992-12-17. Applicant: Siemens Medical Solutions USA, Inc.. Device class: 2.

Clearance details

Applicant: Siemens Medical Solutions USA, Inc.
Product code: Code IXK
Device class: Class 2
Regulation: 21 CFR 892.1630
Advisory panel: Radiology
Date received: 1992-09-02
Decision date: 1992-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Iselin, NJ, US

Download summary PDF View on FDA.gov ↗

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