Catalog Number

-

Brand Name

SPECTRALIS

Version/Model Number

Product Family SW V6.8-US

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 22, 2017

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

K152205

Product Code

MYC

Product Code Name

Ophthalmoscope,Laser,Scanning

Public Device Record Key

1dc660c4-34fe-4aae-b5a6-41bbab7a48bb

Public Version Date

February 19, 2021

Public Version Number

5

DI Record Publish Date

June 12, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-