MODELS 4100 AND 4300 MULTITHERAPY— 510(k) K945954

Name: FDA 510(k) clearance K945954
Creator: U.S. Food and Drug Administration
Published: 1995-01-19

Substantially Equivalent

Spinalight, Inc.

FDA 510(k) clearance K945954 for MODELS 4100 AND 4300 MULTITHERAPY, Substantially Equivalent on 1995-01-19. Applicant: Spinalight, Inc.. Device class: 2.

Clearance details

Applicant: Spinalight, Inc.
Product code: Code JFB
Device class: Class 2
Regulation: 21 CFR 890.5880
Advisory panel: Physical Medicine
Date received: 1994-12-06
Decision date: 1995-01-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woodstock, GA, US

Download summary PDF View on FDA.gov ↗

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