EURO TECH STERLING ROLLER TABLE— 510(k) K943973

Name: FDA 510(k) clearance K943973
Creator: U.S. Food and Drug Administration
Published: 1994-09-29

Substantially Equivalent

Progressive Electrical Therapeutics

FDA 510(k) clearance K943973 for EURO TECH STERLING ROLLER TABLE, Substantially Equivalent on 1994-09-29. Applicant: Progressive Electrical Therapeutics. Device class: 2.

Clearance details

Applicant: Progressive Electrical Therapeutics
Product code: Code JFB
Device class: Class 2
Regulation: 21 CFR 890.5880
Advisory panel: Physical Medicine
Date received: 1994-08-15
Decision date: 1994-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nevada, MO, US

Download summary PDF View on FDA.gov ↗

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K933197 — THE SIGNATURE SERIES, M IV1995-06-02
K943972 — EURO TECH DIAMOND CHIROPRACTIC TABLE1994-10-11
K943974 — EURO TECH MARQUISE CHIROPRACTIC TABLE1994-09-29
K943975 — EURO TECH PLATINUM CHIROPRACTIC TABLE1994-09-29
K933194 — THE SIGNATURE SERIES, IMC IV1994-07-13

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