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

HOME BILI LIGHTS-MODEL 100

K Number: K850599 · Decision Jun 17, 1985
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
70
Applicant Total
8
Review Days
122

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Basic Information

Device Name
HOME BILI LIGHTS-MODEL 100
K Number
K850599
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5700
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Physician Engineered Products, Inc.
Date Received
February 15, 1985
Decision Date
June 17, 1985
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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Other Clearances by Physician Engineered Products, Inc.

K Number Device Name
K110550 BRIGHT EMBRACE MODEL SBL60
K093618 BILI-MIRROR MODEL BLM-1
K974830 ULTRA BILI LIGHT
K883818 MODIFIED REFLUX REDUCER
K882291 RETROFIT BABY FACE SHIELD (RFS)
K882278 RESUSCITATION BAG CONTROLLER (RBC)
K873700 INSTITUTIONAL BILI LIGHT (IBL)