BACK MASTER— 510(k) K914394

Name: FDA 510(k) clearance K914394
Creator: U.S. Food and Drug Administration
Published: 1991-11-13

Substantially Equivalent

Progressive Electrical Therapeutics

FDA 510(k) clearance K914394 for BACK MASTER, Substantially Equivalent on 1991-11-13. Applicant: Progressive Electrical Therapeutics. Device class: 1.

Clearance details

Applicant: Progressive Electrical Therapeutics
Product code: Code BXB
Device class: Class 1
Regulation: 21 CFR 890.5380
Advisory panel: Physical Medicine
Date received: 1991-10-01
Decision date: 1991-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camdenton, MO, US

Download summary PDF View on FDA.gov ↗

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