Catalog Number

DUP88522

Brand Name

ALGICELL® Ag

Version/Model Number

88522

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)

Yes

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

K080497,K080497

Product Code

FRO

Product Code Name

Dressing, wound, drug

Public Device Record Key

3650bcdf-85cb-4604-a435-1142db0e452c

Public Version Date

July 22, 2021

Public Version Number

3

DI Record Publish Date

October 23, 2018

Package DI Number

30381780491655

Quantity per Package

10

Contains DI Package

10381780491651

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case