Catalog Number

-

Brand Name

Vacuum Pump Tubing

Version/Model Number

14205

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 25, 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"

-

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

K991273,K991273

Product Code

MQE

Product Code Name

Needle, Assisted Reproduction

Public Device Record Key

6f078dc5-46d3-4dee-b36c-614917e94dc3

Public Version Date

September 28, 2020

Public Version Number

4

DI Record Publish Date

September 14, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-