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

Airborne Phototherapy Light

K Number: K160238 · Decision Jun 14, 2016
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
70
Applicant Total
8
Review Days
134

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Basic Information

Device Name
Airborne Phototherapy Light
K Number
K160238
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
880.5700
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
International Biomedical
Date Received
February 1, 2016
Decision Date
June 14, 2016
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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