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

LIFE-MASK INFANT RESUSCITATOR

K Number: K842696 · Decision Jul 27, 1984
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
208
Applicant Total
3
Review Days
16

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Basic Information

Device Name
LIFE-MASK INFANT RESUSCITATOR
K Number
K842696
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5915
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Electronic Monitors, Inc.
Date Received
July 11, 1984
Decision Date
July 27, 1984
Product Code
BTM
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
BTM Ventilator, Emergency, Manual (Resuscitator)

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Other Clearances by Electronic Monitors, Inc.

K Number Device Name
K922393 EMITENS ELECTRODES
K822319 RE1000 HEART RATE MONITOR