ENDOSCOPIC ELECTROSURGICAL FIBEROPTIC PROBE— 510(k) K861331

Substantially Equivalent

Trimedyne, Inc.

FDA 510(k) clearance K861331 for ENDOSCOPIC ELECTROSURGICAL FIBEROPTIC PROBE, Substantially Equivalent on 1986-08-07. Applicant: Trimedyne, Inc..

Clearance details

Applicant: Trimedyne, Inc.
Product code: Code LNK
Advisory panel: General, Plastic Surgery
Date received: 1986-04-09
Decision date: 1986-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

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