HUMEROUS FRACTURE BRACE, ULNA FRACTURE— 510(k) K801788

Name: FDA 510(k) clearance K801788
Creator: U.S. Food and Drug Administration
Published: 1980-08-07

Substantially Equivalent

Hosmer Dorrance Corp.

FDA 510(k) clearance K801788 for HUMEROUS FRACTURE BRACE, ULNA FRACTURE, Substantially Equivalent on 1980-08-07. Applicant: Hosmer Dorrance Corp.. Device class: 1.

Clearance details

Applicant: Hosmer Dorrance Corp.
Product code: Code IQI
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1980-07-29
Decision date: 1980-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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