Comfortcare Compression Support with Magnets Comfortcare Magnetic Insoles

FDA 510(k) K013239 · Med Gen, Inc.

Substantially Equivalent

510(k) numberK013239

Submission

Device name
Comfortcare Compression Support with Magnets Comfortcare Magnetic Insoles
Applicant
Med Gen, Inc.
Boca Raton, FL, US
Received
September 28, 2001
Decision date
November 20, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMQ – Restraint, Protective
Device class
Class I (low risk)
Regulation
21 CFR 880.6760
Specialty
General Hospital

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More from Gillen Industries

510(k)DeviceDecision
K013244Comfortcare Compression Support Witih Magnets and Aegis Microbe Shield Comfortcare…FQM · Traditional 12/07/2001SE

Questions and answers

When was Comfortcare Compression Support with Magnets Comfortcare Magnetic Insoles cleared by the FDA?

Comfortcare Compression Support with Magnets Comfortcare Magnetic Insoles (K013239) received a 510(k) decision of Substantially Equivalent on November 20, 2001, 53 days after the submission was received.

What is the product code of K013239?

The FDA product code is FMQ – Restraint, Protective, a Class I (low risk) device regulated under 21 CFR 880.6760.