Catalog Number

-

Brand Name

Maveric Medical

Version/Model Number

M6422

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

July 29, 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

9097f346-d57c-4ab3-943e-00f45a05b97e

Public Version Date

October 24, 2022

Public Version Number

3

DI Record Publish Date

July 29, 2021

Package DI Number

10850028131159

Quantity per Package

25

Contains DI Package

00850028131152

Package Discontinue Date

July 29, 2099

Package Status

In Commercial Distribution

Package Type

Box