Catalog Number

610-918

Brand Name

Ultra-Pro 3™ Needle Guide

Version/Model Number

610-918

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K093713,K093713

Product Code

ITX

Product Code Name

Transducer, ultrasonic, diagnostic

Public Device Record Key

36aed9a1-dc58-4846-a2e1-e720aa5ccbe2

Public Version Date

June 17, 2022

Public Version Number

8

DI Record Publish Date

August 22, 2017

Package DI Number

00841436104449

Quantity per Package

24

Contains DI Package

10841436104446

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-