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

NUWAV

K Number: K081781 · Decision Jul 9, 2008
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
5
Review Days
15

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Basic Information

Device Name
NUWAV
K Number
K081781
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Laborie Medical Technologies, Corp.
Date Received
June 24, 2008
Decision Date
July 9, 2008
Product Code
IYO
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

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