Catalog Number

ML7050 (-20)

Brand Name

ML7050 (Minus 20)

Version/Model Number

ML7050 (-20)

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

K022982,K022982

Product Code

HNO

Product Code Name

Keratome, Ac-Powered

Public Device Record Key

5d0722d4-62e8-45cd-a0e7-3e5424db73e8

Public Version Date

August 20, 2020

Public Version Number

1

DI Record Publish Date

August 12, 2020

Package DI Number

10850724001381

Quantity per Package

10

Contains DI Package

00850724001384

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box