Catalog Number

-

Brand Name

Lantern Delivery Catheter

Version/Model Number

PXSLIMLAN160STR

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"

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

K152840

Product Code

DQY

Product Code Name

CATHETER, PERCUTANEOUS

Public Device Record Key

64d8f965-497c-45f5-b676-edabab8c66ce

Public Version Date

February 17, 2022

Public Version Number

1

DI Record Publish Date

February 09, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-