UNI-PORT— 510(k) K880543

Name: FDA 510(k) clearance K880543
Creator: U.S. Food and Drug Administration
Published: 1988-07-01

Substantially Equivalent

Surgeon Surgical Instrumentation, Inc.

FDA 510(k) clearance K880543 for UNI-PORT, Substantially Equivalent on 1988-07-01. Applicant: Surgeon Surgical Instrumentation, Inc.. Device class: 1.

Clearance details

Applicant: Surgeon Surgical Instrumentation, Inc.
Product code: Code KYG
Device class: Class 1
Regulation: 21 CFR 886.4360
Advisory panel: Ophthalmic
Date received: 1988-02-09
Decision date: 1988-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Placentia, CA, US

Download summary PDF View on FDA.gov ↗

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