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

BILIBLANKET LIGHT METER

K Number: K910571 · Decision Jul 28, 1992
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
70
Applicant Total
120
Review Days
533

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BILIBLANKET LIGHT METER
K Number
K910571
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5700
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Ohmeda Medical
Date Received
February 11, 1991
Decision Date
July 28, 1992
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LBI), ordered by most recent decision date.

View all

Other Clearances by Ohmeda Medical

K Number Device Name
K123309 GIRAFFE AND PANDA WARMERS
K101788 GIRAFFE OMNIBED
K101778 GIRAFFE INCUBATOR
K090697 MODIFICATION TO: GIRAFFE AND PANDA WARMER
K072157 MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)
K070377 GIRAFFE AND PANDA WARMER
K070210 GIRAFFE AND PANDA T- PIECE RESUSCITATION SYSTEM
K070247 GIRAFFE AND PANDA BAG AND MASK RESUSCITATION SYSTEM
K040068 BILIBLANKET PLUS HIGH OUTPUT PHOTOTHERAPY SYSTEM
K020543 OHMEDA MEDICAL GIRAFFE OMNIBED
Search all 120 clearances from Ohmeda Medical →