BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR— 510(k) K862519

Substantially Equivalent

Bausch & Lomb, Inc.

FDA 510(k) clearance K862519 for BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR, Substantially Equivalent on 1986-07-23. Applicant: Bausch & Lomb, Inc..

Clearance details

Applicant: Bausch & Lomb, Inc.
Product code: Code HOS
Advisory panel: Ophthalmic
Date received: 1986-07-01
Decision date: 1986-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

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