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

INSPIRATORY/EXPIRATORY MUSCLE EXERCIS

K Number: K840418 · Decision Feb 17, 1984
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
20
Review Days
17

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Basic Information

Device Name
INSPIRATORY/EXPIRATORY MUSCLE EXERCIS
K Number
K840418
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Inspiron Corp.
Date Received
January 31, 1984
Decision Date
February 17, 1984
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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K772070 VENTILATOR SETUP, VOLUME
K772069 VOL. VENTILATOR SETUP W/OUT NEBULIZER
K772068 MANIFOLD & NEBULIZER, UNIVERSAL
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