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

SMARTNEEDLE(TM) VASCULAR ACCESS SYSTEM

K Number: K913746 · Decision Dec 17, 1991
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
17
Review Days
118

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Basic Information

Device Name
SMARTNEEDLE(TM) VASCULAR ACCESS SYSTEM
K Number
K913746
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Peripheral Systems Group
Date Received
August 21, 1991
Decision Date
December 17, 1991
Product Code
ITX
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
ITX Transducer, Ultrasonic, Diagnostic

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Other Clearances by Peripheral Systems Group

K Number Device Name
K940804 SMARTNEEDLE VASCULAR ACCESS SYSTEM, MODIFICATION
K934433 VANTAGE DIALTAION CATHETER
K932777 SMARTNEEDLE(R) OVER-THE-NEEDLE CATHETER
K931327 PSG DIRECTIONAL HYDROPHILIC GUIDE WIRE
K915554 HI-TORQUE SPORT-T(TM) GUIDE WIRE
K914979 EDM(R) INFUSION CATHETER
K913941 PSG(TM) 20 GUAGE DOPPLER NEEDLE
K915168 PROFLEX 5
K913477 APEX(TM) PROSTATIC BALLOON DILATION CATHETER
K904984 ADVANCE 418(TM)
Search all 17 clearances from Peripheral Systems Group →