PORTABLE THERAPEUTIX SQUID ACTIVE COLD COMPRESSION DEVICE AND COLD PACK— 510(k) K123829

Name: FDA 510(k) clearance K123829
Creator: U.S. Food and Drug Administration
Published: 2013-04-03

Substantially Equivalent

Portable Therapeutix, LLC

FDA 510(k) clearance K123829 for PORTABLE THERAPEUTIX SQUID ACTIVE COLD COMPRESSION DEVICE AND COLD PACK, Substantially Equivalent on 2013-04-03. Applicant: Portable Therapeutix, LLC. Device class: 2.

Clearance details

Applicant: Portable Therapeutix, LLC
Product code: Code IRP
Device class: Class 2
Regulation: 21 CFR 890.5650
Advisory panel: Physical Medicine
Date received: 2012-12-12
Decision date: 2013-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ashland, MA, US

Download summary PDF View on FDA.gov ↗

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