UNIVIT PROBE— 510(k) K950287

Name: FDA 510(k) clearance K950287
Creator: U.S. Food and Drug Administration
Published: 1995-04-10

Substantially Equivalent

Medical Instrument Development Laboratories, Inc.

FDA 510(k) clearance K950287 for UNIVIT PROBE, Substantially Equivalent on 1995-04-10. Applicant: Medical Instrument Development Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Medical Instrument Development Laboratories, Inc.
Product code: Code HKP
Device class: Class 2
Regulation: 21 CFR 886.4150
Advisory panel: Ophthalmic
Date received: 1995-01-24
Decision date: 1995-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Leandro, CA, US

Download summary PDF View on FDA.gov ↗

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