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

MANUAL JET VENTILATOR (WITH REGULATOR AND GAUGE), MANUAL JET VENTILATOR (WITHOUT REGULATOR AND GAUGE), MODELS BE 183-SUR

K Number: K991785 · Decision Aug 17, 1999
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
99
Applicant Total
45
Review Days
84

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Basic Information

Device Name
MANUAL JET VENTILATOR (WITH REGULATOR AND GAUGE), MANUAL JET VENTILATOR (WITHOUT REGULATOR AND GAUGE), MODELS BE 183-SUR
K Number
K991785
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5925
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Instrumentation Industries, Inc.
Date Received
May 25, 1999
Decision Date
August 17, 1999
Product Code
BTL
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
BTL Ventilator, Emergency, Powered (Resuscitator)

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