Catalog Number

-

Brand Name

VascuLab

Version/Model Number

4040

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K131860

Product Code

JOP

Product Code Name

Transducer, Ultrasonic

Public Device Record Key

d8b00c75-9ee5-4125-9110-aed9b5c2956d

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

May 15, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-