Catalog Number

-

Brand Name

LiquiBand Standard

Version/Model Number

LB0002

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K083531,K083531,K083531

Product Code

MPN

Product Code Name

Tissue Adhesive For The Topical Approximation Of Skin

Public Device Record Key

5303a59e-fbb0-430f-b2c4-3d500f67a431

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 06, 2016

Package DI Number

05036912000871

Quantity per Package

10

Contains DI Package

05036912000321

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Shipper Carton