PERIPHERAL TRANSLUMINAL ARGIOPLASTY— 510(k) K832279

Substantially Equivalent

Sontek Corp.

FDA 510(k) clearance K832279 for PERIPHERAL TRANSLUMINAL ARGIOPLASTY, Substantially Equivalent on 1983-11-14. Applicant: Sontek Corp..

Clearance details

Applicant: Sontek Corp.
Advisory panel: Unknown
Date received: 1983-07-12
Decision date: 1983-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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