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

Hudson RCI Voldyne Volumetric Exerciser

K Number: K182847 · Decision Jul 1, 2019
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
64
Review Days
265

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Basic Information

Device Name
Hudson RCI Voldyne Volumetric Exerciser
K Number
K182847
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Teleflexmedical, Inc.
Date Received
October 9, 2018
Decision Date
July 1, 2019
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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