SUTTER MODEL 6000 HAND CPM DEVICE— 510(k) K945221

Substantially Equivalent

Sutter Corp.

FDA 510(k) clearance K945221 for SUTTER MODEL 6000 HAND CPM DEVICE, Substantially Equivalent on 1995-02-27. Applicant: Sutter Corp..

Clearance details

Applicant: Sutter Corp.
Product code: Code BXB
Advisory panel: Physical Medicine
Date received: 1994-10-26
Decision date: 1995-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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