ACQSIM SIMULATOR/LOCALIZER— 510(k) K923851

Name: FDA 510(k) clearance K923851
Creator: U.S. Food and Drug Administration
Published: 1992-10-27

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K923851 for ACQSIM SIMULATOR/LOCALIZER, Substantially Equivalent on 1992-10-27. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1992-07-31
Decision date: 1992-10-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Highland Heights, OH, US

Download summary PDF View on FDA.gov ↗

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