Catalog Number

202038

Brand Name

ViscoInjector

Version/Model Number

ViscoInjector

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

K050716

Product Code

MRH

Product Code Name

Pump, Infusion, Ophthalmic

Public Device Record Key

e5fd70bb-7ef3-4e1c-ac79-6eaede74b586

Public Version Date

December 08, 2020

Public Version Number

2

DI Record Publish Date

January 28, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-