MULTITUBULAR AIR SPLINT KIT— 510(k) K811704

Name: FDA 510(k) clearance K811704
Creator: U.S. Food and Drug Administration
Published: 1981-07-01

Substantially Equivalent

Roger Cestac & Assoc.

FDA 510(k) clearance K811704 for MULTITUBULAR AIR SPLINT KIT, Substantially Equivalent on 1981-07-01. Applicant: Roger Cestac & Assoc.. Device class: 1.

Clearance details

Applicant: Roger Cestac & Assoc.
Product code: Code IQI
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1981-06-16
Decision date: 1981-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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