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

LULLABY TM WARMER

K Number: K121625 · Decision Sep 14, 2012
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
91
Applicant Total
5
Review Days
105

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Basic Information

Device Name
LULLABY TM WARMER
K Number
K121625
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5130
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wipro GE Healthcare Private, Ltd.
Date Received
June 1, 2012
Decision Date
September 14, 2012
Product Code
FMT
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
FMT Warmer, Infant Radiant

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