Catalog Number

LRP-08

Brand Name

LRP-08

Version/Model Number

LRP-08

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

K934638

Product Code

JOP

Product Code Name

Transducer, Ultrasonic

Public Device Record Key

7d064b9b-6738-4d20-91f8-158ca404c121

Public Version Date

April 07, 2021

Public Version Number

4

DI Record Publish Date

June 29, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-