Pedia-Temp(Tm) Liquid-Circulating Hypo-Hypertherm.

FDA 510(k) K902268 · Seabrook Medical Systems, Inc.

Substantially Equivalent

510(k) numberK902268

Submission

Device name
Pedia-Temp(Tm) Liquid-Circulating Hypo-Hypertherm.
Applicant
Seabrook Medical Systems, Inc.
Cincinnati, OH, US
Received
May 21, 1990
Decision date
June 21, 1990
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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More from Ormed GmbH

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K952086Tropicair Convective Warming BlanketsDWJ · Traditional 09/06/1995SE
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K931203Cool-AidILO · Traditional 02/22/1994SE
K923104Tropic-AirDWJ · Traditional 07/13/1993SE
K914182Golden Thermal(R)ILO · Traditional 10/18/1991SE
K902756Tropi-CoolDWJ · Traditional 10/22/1990SE
K902269Electri-Cool(Tm) Liquid-Circulat. Thermal TherapyILO · Traditional 06/21/1990SE
K882310Dual-Temp(Tm) Cooling/Warming UnitILO · Traditional 09/23/1988SE
K881322Mini-Temp(Tm)DWJ · Traditional 06/22/1988SE
K873699Ecmo-Temp (TM) Blood Warming DeviceDWC · Traditional 12/22/1987SE

Questions and answers

When was Pedia-Temp(Tm) Liquid-Circulating Hypo-Hypertherm. cleared by the FDA?

Pedia-Temp(Tm) Liquid-Circulating Hypo-Hypertherm. (K902268) received a 510(k) decision of Substantially Equivalent on June 21, 1990, 31 days after the submission was received.

What is the product code of K902268?

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