Catalog Number

ML7030 (-10)

Brand Name

ML7030 (Minus 10)

Version/Model Number

ML7030 (-10)

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

K010872,K010872

Product Code

HNO

Product Code Name

Keratome, Ac-Powered

Public Device Record Key

7ee0b4bf-9590-418c-9a31-788b4e4c25e2

Public Version Date

August 18, 2020

Public Version Number

2

DI Record Publish Date

July 21, 2020

Package DI Number

10850724001039

Quantity per Package

10

Contains DI Package

00850724001032

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box