Catalog Number

LBS118-03

Brand Name

3M™ Nexcare™

Version/Model Number

LBS118-03

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

-

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

K955103,K955103

Product Code

KMF

Product Code Name

Bandage, liquid

Public Device Record Key

d0904381-2e88-48a3-9605-1871f9147ca7

Public Version Date

October 26, 2018

Public Version Number

1

DI Record Publish Date

September 25, 2018

Package DI Number

50051131862932

Quantity per Package

4

Contains DI Package

00051131862937

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX