Catalog Number

-

Brand Name

OCEAN

Version/Model Number

2052-300

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 31, 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

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

K043582,K043582

Product Code

CAC

Product Code Name

Apparatus, Autotransfusion

Public Device Record Key

96f66325-66ab-4cfb-9d73-a95442d4cd2e

Public Version Date

October 15, 2020

Public Version Number

5

DI Record Publish Date

September 24, 2015

Package DI Number

20650862104039

Quantity per Package

6

Contains DI Package

00650862104035

Package Discontinue Date

October 31, 2017

Package Status

Not in Commercial Distribution

Package Type

-