Catalog Number

-

Brand Name

Enteral Feeding

Version/Model Number

TLCAP

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K092986,K092986,K092986

Product Code

FMF

Product Code Name

Syringe, Piston

Public Device Record Key

ad29d73b-5e53-47a5-87d2-a80c92fb1487

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

February 22, 2018

Package DI Number

20020451332127

Quantity per Package

50

Contains DI Package

00020451332123

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-