UFR FIBEROPTIC CABLE— 510(k) K972225

Name: FDA 510(k) clearance K972225
Creator: U.S. Food and Drug Administration
Published: 1998-03-18

Substantially Equivalent

Universal Fiberoptic Repair, Inc.

FDA 510(k) clearance K972225 for UFR FIBEROPTIC CABLE, Substantially Equivalent on 1998-03-18. Applicant: Universal Fiberoptic Repair, Inc.. Device class: 2.

Clearance details

Applicant: Universal Fiberoptic Repair, Inc.
Product code: Code FST
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 1997-06-13
Decision date: 1998-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pomfret Center, CT, 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.