BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM— 510(k) K896685

Substantially Equivalent

Bausch & Lomb, Inc.

FDA 510(k) clearance K896685 for BAUSCH & LOMB FREQUENT REPLACEMENT CASE SYSTEM, Substantially Equivalent on 1989-12-26. Applicant: Bausch & Lomb, Inc..

Clearance details

Applicant: Bausch & Lomb, Inc.
Product code: Code LRX
Advisory panel: Ophthalmic
Date received: 1989-11-28
Decision date: 1989-12-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

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