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

IMEX FUTURALDOP PRO

K Number: K970156 · Decision Apr 4, 1997
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
19
Review Days
78

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Basic Information

Device Name
IMEX FUTURALDOP PRO
K Number
K970156
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Imex Medical Systems, Inc.
Date Received
January 16, 1997
Decision Date
April 4, 1997
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 Imex Medical Systems, Inc.

K Number Device Name
K973556 IMEX MEDICAL SYSTEMS, INC. IMEXLAB 9000
K973562 IMEX MEDICAL SYSTEMS, INC. IMEXLAB 9100
K973336 IMEX STETHODOP
K942243 IMEX 8000 PERSONAL CASCULAR LAB
K944196 IMWXDOP IR
K942441 IMEXDOP CT+
K910462 POCKET DOP 3
K901593 IMEX DOP-TONE II
K896613 FLAT VASCULAR PROBE
K882138 IMEXLAB 3000 VASCULAR DIAGNOSTIC RECORDER
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