SCLERAL PLUG— 510(k) K831193

Name: FDA 510(k) clearance K831193
Creator: U.S. Food and Drug Administration
Published: 1983-06-30

Substantially Equivalent

Medical Instrument Development Laboratories, Inc.

FDA 510(k) clearance K831193 for SCLERAL PLUG, Substantially Equivalent on 1983-06-30. Applicant: Medical Instrument Development Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Medical Instrument Development Laboratories, Inc.
Product code: Code LXP
Device class: Class 2
Regulation: 21 CFR 886.4155
Advisory panel: Ophthalmic
Date received: 1983-04-12
Decision date: 1983-06-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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