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

TP Pivot Pro™ Needle Guide

K Number: K233109 · Decision Dec 22, 2023
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
2
Review Days
86

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Basic Information

Device Name
TP Pivot Pro™ Needle Guide
K Number
K233109
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Civco Medical Solutions
Date Received
September 27, 2023
Decision Date
December 22, 2023
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 Civco Medical Solutions

K Number Device Name
K190802 Envision ultrasound pad and cover