Catalog Number

MC1755M2U

Brand Name

PROWLER

Version/Model Number

MC1755M2U

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

K214025

Product Code

DQY

Product Code Name

Catheter, percutaneous

Public Device Record Key

d9a74a93-9341-4293-a7f9-8e7fdc0f84f4

Public Version Date

October 07, 2022

Public Version Number

2

DI Record Publish Date

May 24, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-