Catalog Number

1130

Brand Name

PearlFit Head/Neck Vac

Version/Model Number

PearlFit Head/Neck Vac

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

-

Product Code

KXH

Product Code Name

Cradle, Patient, Radiologic

Public Device Record Key

efee3408-d2a1-4f9c-b03f-baca1cf7d87a

Public Version Date

May 19, 2022

Public Version Number

1

DI Record Publish Date

May 11, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-