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

MOUTH TO FACE RESUSCITATOR

K Number: K873043 · Decision Sep 28, 1987
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
208
Applicant Total
7
Review Days
55

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Basic Information

Device Name
MOUTH TO FACE RESUSCITATOR
K Number
K873043
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5915
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Artec Environmental Monitoring Division
Date Received
August 4, 1987
Decision Date
September 28, 1987
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)

Similar 510(k) Clearances

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

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Other Clearances by Artec Environmental Monitoring Division

K Number Device Name
K900839 THE CAROLINA ROCKER
K896886 ARTEC RESPOND PULMONARY RESUSCITATOR
K863910 RAINCOAT
K854573 ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE
K832512 AIRWAY MASKS
K830056 ARTEC TWIST VALVE