Catalog Number

LG003M

Brand Name

CALICO

Version/Model Number

LG003M

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K212309,K212309,K212309

Product Code

LZA

Product Code Name

Polymer Patient Examination Glove

Public Device Record Key

4dab14f0-ccc5-4684-b007-f1ca4cbfac43

Public Version Date

August 25, 2022

Public Version Number

1

DI Record Publish Date

August 17, 2022

Package DI Number

20850044458312

Quantity per Package

10

Contains DI Package

00850044458318

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case