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

VMA PEDIATRIC APNEA MATTRESS

K Number: K811865 · Decision Jul 31, 1981
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
174
Applicant Total
22
Review Days
30

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Basic Information

Device Name
VMA PEDIATRIC APNEA MATTRESS
K Number
K811865
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vickers America Medical Corp.
Date Received
July 1, 1981
Decision Date
July 31, 1981
Product Code
BZQ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BZQ Monitor, Breathing Frequency

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K813239 OXYGENAIRE NURING INCUBATOR
K813238 NEOCARE BABY-CONTROLLED INCUBATOR
K810792 NEOCARE TEMPERATURE MONITOR
K810067 140 NEOCARE AIR CONTROLLED INCUBATOR
K810571 NEOCARE OXYGEN MONITOR
K802251 SP 120 SOPHISTICATE
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