BAUSCH & LOMB CONTACT LENS VIEWER— 510(k) K862517

Name: FDA 510(k) clearance K862517
Creator: U.S. Food and Drug Administration
Published: 1986-08-11

Substantially Equivalent

Bausch & Lomb, Inc.

FDA 510(k) clearance K862517 for BAUSCH & LOMB CONTACT LENS VIEWER, Substantially Equivalent on 1986-08-11. Applicant: Bausch & Lomb, Inc.. Device class: 1.

Clearance details

Applicant: Bausch & Lomb, Inc.
Product code: Code HLF
Device class: Class 1
Regulation: 21 CFR 886.1430
Advisory panel: Ophthalmic
Date received: 1986-07-01
Decision date: 1986-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rochester, NY, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.