Catalog Number

PH-270-70-S + PH-K-A

Brand Name

PHASOR

Version/Model Number

PH-270-70-S + PH-K-A

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

November 28, 2120

Issuing Agency

In HIBCC

MRI safety Status

MR Unsafe

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

-

Product Code

-

Product Code Name

-

Public Device Record Key

0c0164a6-d440-4117-8203-d768f3e5da89

Public Version Date

December 07, 2020

Public Version Number

1

DI Record Publish Date

November 29, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-