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

INCENTIVE SPIROMETER

K Number: K000314 · Decision Apr 12, 2000
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
22
Review Days
71

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Basic Information

Device Name
INCENTIVE SPIROMETER
K Number
K000314
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Engineered Medical Systems
Date Received
February 1, 2000
Decision Date
April 12, 2000
Product Code
BWF
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
BWF Spirometer, Therapeutic (Incentive)

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