Catalog Number

2121

Brand Name

LiteTouch

Version/Model Number

2121

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

March 06, 2026

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)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K132553,K132553,K132553

Product Code

FMF

Product Code Name

Syringe, Piston

Public Device Record Key

4c32e88c-8451-400a-90e1-4b491067b182

Public Version Date

March 15, 2021

Public Version Number

1

DI Record Publish Date

March 06, 2021

Package DI Number

10732671121216

Quantity per Package

20

Contains DI Package

00732671021212

Package Discontinue Date

March 06, 2026

Package Status

In Commercial Distribution

Package Type

Form Fill Seal Tray