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

AIDA VI.8 DIAGNOSTIC ULTRASOUND GM-72P00A, L13-5V1 TRANSDUCER

K Number: K122009 · Decision Oct 3, 2012
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
1171
Applicant Total
3
Review Days
86

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Basic Information

Device Name
AIDA VI.8 DIAGNOSTIC ULTRASOUND GM-72P00A, L13-5V1 TRANSDUCER
K Number
K122009
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1550
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Panasonic Healthcare Co., Ltd.
Date Received
July 9, 2012
Decision Date
October 3, 2012
Product Code
IYN
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
IYN System, Imaging, Pulsed Doppler, Ultrasonic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IYN), ordered by most recent decision date.

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Other Clearances by Panasonic Healthcare Co., Ltd.

K Number Device Name
K113612 AIDA V1.5 DIAGNOSTIC ULTRASOUND SYSTEM GM-72P00A
K103148 AIDA DIAGNOSTIC ULTRASOUND SYSTEM