Catalog Number

-

Brand Name

GenetiSure Dx Wash Buffer 1

Version/Model Number

K1201-64305

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

K163367

Product Code

PFX

Product Code Name

System, microarray-based, genome-wide, postnatal chromosomal abnormality detection

Public Device Record Key

e6c3b341-b89d-4d2e-afda-e809c2f82197

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 07, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-