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

BABYTHERM 8000 WB

K Number: K945467 · Decision Apr 28, 1995
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
92
Applicant Total
20
Review Days
172

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Basic Information

Device Name
BABYTHERM 8000 WB
K Number
K945467
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5720
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Drager, Inc.
Date Received
November 7, 1994
Decision Date
April 28, 1995
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

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K974176 BABYLOG 8000 PLUS
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K970165 EVITA 2 DURA
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