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

OHMEDA CONTINUOUS SUCTION REGULATOR

K Number: K883229 · Decision Oct 19, 1988
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
20
Applicant Total
120
Review Days
79

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Basic Information

Device Name
OHMEDA CONTINUOUS SUCTION REGULATOR
K Number
K883229
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Ohmeda Medical
Date Received
August 1, 1988
Decision Date
October 19, 1988
Product Code
KDP
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
KDP Regulator, Vacuum

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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 →