BEACON-P, MODEL 211059— 510(k) K992335

Name: FDA 510(k) clearance K992335
Creator: U.S. Food and Drug Administration
Published: 1999-10-07

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K992335 for BEACON-P, MODEL 211059, Substantially Equivalent on 1999-10-07. Applicant: Philips Medical Systems (Cleveland), Inc.. Device class: 2.

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 1999-07-13
Decision date: 1999-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cleveland, OH, US

Download summary PDF View on FDA.gov ↗

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