Catalog Number

-

Brand Name

AMPLATZ GOOSE NECK™

Version/Model Number

MC4000

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

K972511

Product Code

DXE

Product Code Name

Catheter, embolectomy

Public Device Record Key

2616a3f2-8606-4929-bb07-6f35a4c3262d

Public Version Date

July 08, 2021

Public Version Number

2

DI Record Publish Date

November 13, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-