Catalog Number

0210918000

Brand Name

InterPulse

Version/Model Number

0210918000

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

Yes

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

-

Product Code

FQH

Product Code Name

LAVAGE, JET

Public Device Record Key

c324921c-aca7-46e4-b532-2e14b47a7bc2

Public Version Date

November 06, 2020

Public Version Number

4

DI Record Publish Date

September 23, 2016

Package DI Number

37613154730217

Quantity per Package

6

Contains DI Package

07613154730216

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

pack