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

EMT-CPAP

K Number: K021520 · Decision Jul 15, 2002
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
99
Applicant Total
1
Review Days
66

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Basic Information

Device Name
EMT-CPAP
K Number
K021520
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5925
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Emergency Medical Techology
Date Received
May 10, 2002
Decision Date
July 15, 2002
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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