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

MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 2000EZ

K Number: K040367 · Decision Apr 7, 2004
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
57
Applicant Total
5
Review Days
54

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Basic Information

Device Name
MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 2000EZ
K Number
K040367
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5665
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Electromed, Inc.
Date Received
February 13, 2004
Decision Date
April 7, 2004
Product Code
BYI
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
BYI Percussor, Powered-Electric

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