Catalog Number

-

Brand Name

MEDLOCK

Version/Model Number

MM13150-10

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K172344,K172344

Product Code

KNW

Product Code Name

Instrument, Biopsy

Public Device Record Key

16fc4c20-cf81-430f-a061-8a06deacfe7f

Public Version Date

July 06, 2018

Public Version Number

2

DI Record Publish Date

April 10, 2018

Package DI Number

18056772675822

Quantity per Package

10

Contains DI Package

08056772675825

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-