Catalog Number

091XP

Brand Name

Lac-Mac

Version/Model Number

091XP

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K031362

Product Code

KKX

Product Code Name

Drape, Surgical

Public Device Record Key

b777fc61-4b22-4d6a-801f-9cdf50d7c8ff

Public Version Date

November 16, 2021

Public Version Number

1

DI Record Publish Date

November 08, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-