Catalog Number

896634003

Brand Name

TRUWAVE

Version/Model Number

PX1800

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K142749

Product Code

DXO

Product Code Name

TRANSDUCER, PRESSURE, CATHETER TIP

Public Device Record Key

fb160e3b-9c72-43e0-9dca-d79f92307202

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 03, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-