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

THERMAL REGULATION SYSTEM BLANKET

K Number: K964377 · Decision Apr 23, 1997
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
157
Applicant Total
15
Review Days
173

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Basic Information

Device Name
THERMAL REGULATION SYSTEM BLANKET
K Number
K964377
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Gibeck, Inc.
Date Received
November 1, 1996
Decision Date
April 23, 1997
Product Code
DWJ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DWJ System, Thermal Regulating

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Other Clearances by Gibeck, Inc.

K Number Device Name
K965016 ISO-GARD FILTER ANGLED(18212)/ISO-GARD FILTER STRAIGHT(19212)
K964382 HUMID-VENT FILTER COMPACT ANGLED (18402)/HUMID-VENT FILTER COMPACT STRAIGHT(19402)
K960511 GIBECK WARMBAG REUSABLE CONVECTIVE WARMING BLANKET
K954828 ISO-GARD HEPA FILTER-HME, ISO-ARD HEPA FILTER-HME W/PORT
K953544 HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT
K953491 HUMID-VENT 1 PORT/HUMID-VENT 1 PORT ANGLE
K952845 HUMID-VENT TRACH-VENT
K952844 HUMID-VENT 2
K952750 HUMID-VENT 1
K952084 HUMID-VENT FILTER PEDI
Search all 15 clearances from Gibeck, Inc. →