EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391— 510(k) K971570

Substantially Equivalent

Quinton Electrophysiology Corp.

FDA 510(k) clearance K971570 for EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391, Substantially Equivalent on 1997-12-29. Applicant: Quinton Electrophysiology Corp..

Clearance details

Applicant: Quinton Electrophysiology Corp.
Product code: Code DRR
Advisory panel: Cardiovascular
Date received: 1997-04-29
Decision date: 1997-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

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