Catalog Number

1014933

Brand Name

OPTIS™

Version/Model Number

1014933

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NQQ

Product Code Name

SYSTEM, IMAGING, OPTICAL COHERENCE TOMOGRAPHY (OCT)

Public Device Record Key

158d0922-7326-48b7-b88c-f9fdbe6e6e53

Public Version Date

June 24, 2021

Public Version Number

1

DI Record Publish Date

June 16, 2021

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-