ULTRALITE HF1236 HAND AND FOOT SYSTEM— 510(k) K861963

Name: FDA 510(k) clearance K861963
Creator: U.S. Food and Drug Administration
Published: 1986-06-25

Substantially Equivalent

Ultralite

FDA 510(k) clearance K861963 for ULTRALITE HF1236 HAND AND FOOT SYSTEM, Substantially Equivalent on 1986-06-25. Applicant: Ultralite. Device class: 2.

Clearance details

Applicant: Ultralite
Product code: Code FTC
Device class: Class 2
Regulation: 21 CFR 878.4630
Advisory panel: General, Plastic Surgery
Date received: 1986-05-20
Decision date: 1986-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lawrenceville, GA, US

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