Catalog Number

-

Brand Name

N/A

Version/Model Number

ULTRASOUND TRANSDUCER WATERTIGHT LOOP

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

K982651

Product Code

HEL

Product Code Name

MONITOR, HEART RATE, FETAL, ULTRASONIC

Public Device Record Key

ff1cf68e-43a3-4297-b406-00fb8976ec4a

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

June 24, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-