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

RESUSCI-BAG-VALVE

K Number: K791468 · Decision Aug 22, 1979
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
208
Applicant Total
83
Review Days
16

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Basic Information

Device Name
RESUSCI-BAG-VALVE
K Number
K791468
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5915
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Concept, Inc.
Date Received
August 6, 1979
Decision Date
August 22, 1979
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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