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

BAGEASY(R) III CHILD/INFANT DISPOS MAN RESUSCITATORS

K Number: K940581 · Decision May 6, 1994
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
208
Applicant Total
172
Review Days
87

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Basic Information

Device Name
BAGEASY(R) III CHILD/INFANT DISPOS MAN RESUSCITATORS
K Number
K940581
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5915
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Respironics, Inc.
Date Received
February 8, 1994
Decision Date
May 6, 1994
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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