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

OXYGENAIRE NURING INCUBATOR

K Number: K813239 · Decision Jan 28, 1982
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
84
Applicant Total
22
Review Days
72

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Basic Information

Device Name
OXYGENAIRE NURING INCUBATOR
K Number
K813239
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5400
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Vickers America Medical Corp.
Date Received
November 17, 1981
Decision Date
January 28, 1982
Product Code
FMZ
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
FMZ Incubator, Neonatal

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Other Clearances by Vickers America Medical Corp.

K Number Device Name
K840823 TREONIC C30
K831838 LABORATORY DATA MGMT SYSTEM SDMS
K830748 RESUSCITAIRE
K830936 TREONIC IP5
K813238 NEOCARE BABY-CONTROLLED INCUBATOR
K811865 VMA PEDIATRIC APNEA MATTRESS
K810792 NEOCARE TEMPERATURE MONITOR
K810067 140 NEOCARE AIR CONTROLLED INCUBATOR
K810571 NEOCARE OXYGEN MONITOR
K802251 SP 120 SOPHISTICATE
Search all 22 clearances from Vickers America Medical Corp. →