Catalog Number

-

Brand Name

Maveric Medical

Version/Model Number

M6250

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

September 25, 2099

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

K172763,K172763,K172763

Product Code

JKA

Product Code Name

Tubes, Vials, Systems, Serum Separators, Blood Collection

Public Device Record Key

04f097e4-46e0-4c38-a86f-a4e6785a3d52

Public Version Date

October 24, 2022

Public Version Number

2

DI Record Publish Date

September 24, 2021

Package DI Number

10850028131029

Quantity per Package

50

Contains DI Package

00850028131022

Package Discontinue Date

September 25, 2099

Package Status

In Commercial Distribution

Package Type

Box