BOGER AUTO-TRACTION DEVICE— 510(k) K820663

Name: FDA 510(k) clearance K820663
Creator: U.S. Food and Drug Administration
Published: 1982-05-03

Substantially Equivalent

D.C. Medical Device, Inc.

FDA 510(k) clearance K820663 for BOGER AUTO-TRACTION DEVICE, Substantially Equivalent on 1982-05-03. Applicant: D.C. Medical Device, Inc.. Device class: 1.

Clearance details

Applicant: D.C. Medical Device, Inc.
Product code: Code ILZ
Device class: Class 1
Regulation: 21 CFR 890.5925
Advisory panel: Physical Medicine
Date received: 1982-03-10
Decision date: 1982-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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