SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG— 510(k) K941869

Name: FDA 510(k) clearance K941869
Creator: U.S. Food and Drug Administration
Published: 1994-08-03

Substantially Equivalent

The Lighthouse For the Blind, Inc.

FDA 510(k) clearance K941869 for SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG, Substantially Equivalent on 1994-08-03. Applicant: The Lighthouse For the Blind, Inc.. Device class: 1.

Clearance details

Applicant: The Lighthouse For the Blind, Inc.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1994-04-18
Decision date: 1994-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seattle, WA, US

Download summary PDF View on FDA.gov ↗

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