Themalator. Models T-4-S, T-8-S, Etc.

FDA 510(k) K950350 · Whitehall/Div Columbus Mckennon Corp.

Substantially Equivalent

510(k) numberK950350

Submission

Device name
Themalator. Models T-4-S, T-8-S, Etc.
Applicant
Whitehall/Div Columbus Mckennon Corp.
City Of Industry, CA, US
Received
January 30, 1995
Decision date
March 24, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IRQ – Unit, Heating, Powered
Device class
Class I (low risk)
Regulation
21 CFR 890.5950
Specialty
Physical Medicine

Other 510(k)s with product code IRQ

510(k)DeviceApplicantDecision
K050524Ez-Iv Medical Pad Warming Unit, Model 1000IRQ · Traditional Marda Medical, Inc.09/14/2005SE
K924023Ferno Ille Inferno Moist Heat Therapy Ut, 916/917IRQ · Traditional Ferno04/14/1993SE
K880644Ultra-Pan for Orthotic Plastics (7262)IRQ · Traditional Fred Sammons, Inc.05/06/1988SE
K861340R1750 and R1424 Powered Heating UnitsIRQ · Traditional Tri W-G, Inc.05/02/1986SE
K832177Pulsair Model SP-1IRQ · Traditional Thermowave Medical Device Corp.12/09/1983SE
K801625Thermolator Heating UnitIRQ · Traditional Tru-Eze Mfg. Co., Inc.07/28/1980SE

Questions and answers

When was Themalator. Models T-4-S, T-8-S, Etc. cleared by the FDA?

Themalator. Models T-4-S, T-8-S, Etc. (K950350) received a 510(k) decision of Substantially Equivalent on March 24, 1995, 53 days after the submission was received.

What is the product code of K950350?

The FDA product code is IRQ – Unit, Heating, Powered, a Class I (low risk) device regulated under 21 CFR 890.5950.