Catalog Number

HJ3202T

Brand Name

HoverJack

Version/Model Number

HJ3202T

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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"

Yes

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K041503

Product Code

FNG

Product Code Name

LIFT, PATIENT, AC-POWERED

Public Device Record Key

ac2c4c90-2bb7-48a1-9d19-2e9977fb4c0e

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

July 30, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-