Hot/Ice Disposable Blanket

FDA 510(k) K833564 · Thermo Temp, Inc.

Substantially Equivalent

510(k) numberK833564

Submission

Device name
Hot/Ice Disposable Blanket
Applicant
Thermo Temp, Inc.
Mchenry, IL, US
Received
October 12, 1983
Decision date
November 28, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
ILO – Pack, Hot Or Cold, Water Circulating
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5720
Specialty
Physical Medicine

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K070402Modification to Polar Care 500ILO · Special Breg, Inc.03/29/2007SE
K040317Ivc SystemILO · Traditional Mark H. Friedman05/07/2004SE
K973023Incare Hot/Ice System Foot/Ankle BlanketILO · Traditional Hollister, Inc.11/03/1997SE
K970197HTP-1500 Localized Heat Therapy PumpILO · Traditional Adroit Medical Systems, Inc.09/10/1997SE
K964799Artrotherm Cryotherapy and ThernotherapyILO · Traditional Ormed GmbH08/29/1997SE
K964354Artocool-S Water Circulating Cold PackILO · Traditional Ormed GmbH08/29/1997SE

More from Ormed GmbH

510(k)DeviceDecision
K871963Hot/Ice Disposable BlanketILO · Traditional 06/26/1987SE
K871962Hot/Ice Dual Function EquipmentILO · Traditional 06/26/1987SE
K830757Hot/IceILO · Traditional 03/29/1983SE

Questions and answers

When was Hot/Ice Disposable Blanket cleared by the FDA?

Hot/Ice Disposable Blanket (K833564) received a 510(k) decision of Substantially Equivalent on November 28, 1983, 47 days after the submission was received.

What is the product code of K833564?

The FDA product code is ILO – Pack, Hot Or Cold, Water Circulating, a Class II (moderate risk) device regulated under 21 CFR 890.5720.