Catalog Number

-

Brand Name

AUTO REFKERATOMETER

Version/Model Number

RC-5000

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

-

Product Code

HKO

Product Code Name

Refractometer, Ophthalmic

Public Device Record Key

cd670a68-c2c3-411e-84f9-760230ed6e8f

Public Version Date

April 11, 2022

Public Version Number

1

DI Record Publish Date

April 01, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-