FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DUAL-TEMP(TM) COOLING/WARMING UNIT

K Number: K882310 · Decision Sep 23, 1988
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
92
Applicant Total
12
Review Days
112

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DUAL-TEMP(TM) COOLING/WARMING UNIT
K Number
K882310
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5720
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Seabrook Medical Systems, Inc.
Date Received
June 3, 1988
Decision Date
September 23, 1988
Product Code
ILO
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ILO Pack, Hot Or Cold, Water Circulating

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ILO), ordered by most recent decision date.

View all

Other Clearances by Seabrook Medical Systems, Inc.

K Number Device Name
K946196 TROPICAIR CONVECTIVE WARING SYSTEM
K952086 TROPICAIR CONVECTIVE WARMING BLANKETS
K931203 COOL-AID
K923104 TROPIC-AIR
K914182 GOLDEN THERMAL(R)
K902756 TROPI-COOL
K902269 ELECTRI-COOL(TM) LIQUID-CIRCULAT. THERMAL THERAPY
K902268 PEDIA-TEMP(TM) LIQUID-CIRCULATING HYPO-HYPERTHERM.
K881322 MINI-TEMP(TM)
K873699 ECMO-TEMP (TM) BLOOD WARMING DEVICE
Search all 12 clearances from Seabrook Medical Systems, Inc. →