Catalog Number

CAFK-901

Brand Name

Coda®

Version/Model Number

CAFK-901

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

-

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

K001486,K001486

Product Code

MQG

Product Code Name

ACCESSORY, ASSISTED REPRODUCTION

Public Device Record Key

1061be5e-adc8-4e43-ad09-31d5b3767f3e

Public Version Date

February 06, 2020

Public Version Number

4

DI Record Publish Date

September 21, 2016

Package DI Number

00815965021409

Quantity per Package

2

Contains DI Package

00815965021355

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

2-pack, CAFK-900