ENDOSCOPIC FIBEROPTIC CABLE— 510(k) K991208

Substantially Equivalent

Isolux America

FDA 510(k) clearance K991208 for ENDOSCOPIC FIBEROPTIC CABLE, Substantially Equivalent on 1999-06-23. Applicant: Isolux America.

Clearance details

Applicant: Isolux America
Product code: Code HBI
Advisory panel: General, Plastic Surgery
Date received: 1999-04-09
Decision date: 1999-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, US

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