MENTOR ANTERIOR SEGMENT VITRECTOR— 510(k) K890595

Name: FDA 510(k) clearance K890595
Creator: U.S. Food and Drug Administration
Published: 1989-04-17

Substantially Equivalent

Mentor O & O, Inc.

FDA 510(k) clearance K890595 for MENTOR ANTERIOR SEGMENT VITRECTOR, Substantially Equivalent on 1989-04-17. Applicant: Mentor O & O, Inc.. Device class: 2.

Clearance details

Applicant: Mentor O & O, Inc.
Product code: Code HKP
Device class: Class 2
Regulation: 21 CFR 886.4150
Advisory panel: Ophthalmic
Date received: 1989-02-06
Decision date: 1989-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwell, MA, US

Download summary PDF View on FDA.gov ↗

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