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

SHAPEABLE DOPPLER FLOW PROBE

K Number: K002958 · Decision Dec 18, 2001
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
12
Review Days
452

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Basic Information

Device Name
SHAPEABLE DOPPLER FLOW PROBE
K Number
K002958
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cook Vascular, Inc.
Date Received
September 22, 2000
Decision Date
December 18, 2001
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 Cook Vascular, Inc.

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K141148 EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET, EVOLUTION SHORTIE RL CONTROLLED-ROTATION DILATOR SHEATH SET
K110347 DOPPLER MONITOR
K083482 COOK VASCULAR VITAL-JECT POWER INJECTABLE SAFETY INFUSION SET
K081425 COOK VASCULAR INC. VITAL-PORT VASCULAR ACCESS SYSTEM POWER INJECTABLE PORT
K061000 EVOLUTION MECHANICAL DILATOR SHEATH SET MODELS-LR-EVN-7.0, LR-EVN-9.0
K032223 COOK VASCULAR PERFECTA ELECTROSURGICAL DISSECTION SYSTEM ERGONOMIC INTERMITTENT ACTIVATION SWITCH
K023937 COOK VASCULAR SERPENTA CORONARY SINUS INTRODUCER SYSTEM
K022649 COOK-SWARTZ DOPPLER FLOW PROBE
K010128 COOK VASCULAR PEEL-AWAY HEMOSTASIS VALVE
Search all 12 clearances from Cook Vascular, Inc. →