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

TRINGA ULTRASOUND IMAGING SYSTEM, MODEL 50L

K Number: K033604 · Decision Dec 15, 2003
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
12
Review Days
28

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Basic Information

Device Name
TRINGA ULTRASOUND IMAGING SYSTEM, MODEL 50L
K Number
K033604
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pie Medical
Date Received
November 17, 2003
Decision Date
December 15, 2003
Product Code
IYO
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

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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Other Clearances by Pie Medical

K Number Device Name
K061961 ART LAB SOFTWARE
K053154 MYLAB15/20 3D/4D ULTRASOUND IMAGING SYSTEM
K043588 MYLAB 15 / MYLAB 20, MODEL 2700
K043360 IMT.LAB
K041675 PICUS, PARUS, FALCO AND AQUILA ULTRASOUND SYSTEMS
K023512 PICUS ULTRASOUND IMAGING SYSTEMS
K020112 50S TRINGA ULTRASOUND IMAGING SYSTEM
K003725 240 PARUS ULTRASOUND IMAGING SYSTEMS, MODEL 240 PARUS
K003292 260 CORVUS
K002357 100 S AND 100 LC AND 485 ANSER ULTRASOUND IMAGING SYSTEMS
Search all 12 clearances from Pie Medical →