Catalog Number

VPC0648

Brand Name

OPTICS ONE

Version/Model Number

VPC0648

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"

Yes

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

-

Product Code

KKX

Product Code Name

Drape, Surgical

Public Device Record Key

e51202cd-b470-4b8e-9d63-84c4cbd59a32

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

November 07, 2017

Package DI Number

00815384023565

Quantity per Package

20

Contains DI Package

00815384023558

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE