SUTURE REMOVAL KIT— 510(k) K922339

Unknown

Transidyne General Corp.

FDA 510(k) clearance K922339 for SUTURE REMOVAL KIT, Unknown on 1992-12-11. Applicant: Transidyne General Corp..

Clearance details

Applicant: Transidyne General Corp.
Product code: Code MCZ
Advisory panel: General, Plastic Surgery
Date received: 1992-05-19
Decision date: 1992-12-11
Decision: Unknown
Clearance type: Traditional
Location: Spartanburg, SC, US

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