CATARACT LIQUEFRACTURE DEVICE— 510(k) K980292

Substantially Equivalent

Alcon Laboratories

FDA 510(k) clearance K980292 for CATARACT LIQUEFRACTURE DEVICE, Substantially Equivalent on 1998-05-19. Applicant: Alcon Laboratories.

Clearance details

Applicant: Alcon Laboratories
Product code: Code MUS
Advisory panel: Ophthalmic
Date received: 1998-01-26
Decision date: 1998-05-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Worth, TX, US

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