Catalog Number

4740

Brand Name

Accuro Instrument Cover Kit

Version/Model Number

2040

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K970889,K970889

Product Code

KKX

Product Code Name

Drape, Surgical

Public Device Record Key

510dd1c8-a72a-48bd-83ba-0b147825ebe7

Public Version Date

May 18, 2021

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

10841912100139

Quantity per Package

24

Contains DI Package

00841912100132

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-