Catalog Number

-

Brand Name

PECO

Version/Model Number

PU010

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 10, 2020

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K111405,K111405

Product Code

GBM

Product Code Name

CATHETER, URETHRAL

Public Device Record Key

807d1841-6acd-473a-b088-0eba58ec6e0e

Public Version Date

August 17, 2021

Public Version Number

4

DI Record Publish Date

September 08, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-