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

DRAGER PT4000 PHOTOTHERAPY SYSTEM

K Number: K954611 · Decision Dec 1, 1995
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
70
Applicant Total
20
Review Days
58

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Basic Information

Device Name
DRAGER PT4000 PHOTOTHERAPY SYSTEM
K Number
K954611
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5700
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Drager, Inc.
Date Received
October 4, 1995
Decision Date
December 1, 1995
Product Code
LBI
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
LBI Unit, Neonatal Phototherapy

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K982789 MEDICAL AIR COMPRESSOR, MODEL # 8413419
K980642 EVITA 4 (8411900)
K974176 BABYLOG 8000 PLUS
K971198 BABYTHERM 8004 BABYTHERM 8010
K970165 EVITA 2 DURA
K954204 DRAGER INCUBATOR 8000 IC
K961687 EVITA 4
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