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

22 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CATHETER/NEEDLE ASSEMBLY), 24 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CAR

K Number: K973713 · Decision Jan 23, 1998
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
11
Review Days
116

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Basic Information

Device Name
22 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CATHETER/NEEDLE ASSEMBLY), 24 GAUGE P.D. ACCESS VASCULAR ACCESS DEVICE (CAR
K Number
K973713
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardiovascular Dynamics, Inc.
Date Received
September 29, 1997
Decision Date
January 23, 1998
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 Cardiovascular Dynamics, Inc.

K Number Device Name
K971577 FOCUS-PV BALLOON DILATATION CATHETER
K963989 P.D. ACCESS (PERCUTANEOUS DOPPLER) VASCULAR ACCESS DEVICE
K963688 FOCUS PV BALLOON DILATATION CATHETER
K945693 CVD PERIFLOW(TM) (SMALL VESSEL) BALLOON DILATATION CATHETER
K952064 FOCUS BALLOON DILATATION CATHETER
K951502 CVD BULLET INFUSION CATYHETER
K951503 CVD BULLETT HI-FLO INFUSION CATHETER
K944016 FOCUS BALLOON DILATATION CATHETER
K945465 CVD SMALL VESSEL BALLOON DILATATION CATHETER
K943023 CVD BULLETT PERIPHERAL INFUSION CATHETER
Search all 11 clearances from Cardiovascular Dynamics, Inc. →