Catalog Number

-

Brand Name

Wavelength

Version/Model Number

NTPF900X

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

K012522

Product Code

MUI

Product Code Name

Media, Coupling, Ultrasound

Public Device Record Key

b4f0f0d7-258a-44c9-a914-729c38929168

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

December 21, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-