LEKSELL GAMMAPLAN— 510(k) K973441

Name: FDA 510(k) clearance K973441
Creator: U.S. Food and Drug Administration
Published: 1998-04-01

Substantially Equivalent

Patterson Consulting Group, Inc.

FDA 510(k) clearance K973441 for LEKSELL GAMMAPLAN, Substantially Equivalent on 1998-04-01. Applicant: Patterson Consulting Group, Inc.. Device class: 2.

Clearance details

Applicant: Patterson Consulting Group, Inc.
Product code: Code IWB
Device class: Class 2
Regulation: 21 CFR 892.5750
Advisory panel: Radiology
Date received: 1997-09-11
Decision date: 1998-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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