Catalog Number

HOTSHOT

Brand Name

Hotshot™ Controller

Version/Model Number

HOTSHOT

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

December 31, 2022

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

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

K214114

Product Code

QEW

Product Code Name

Peripheral Mechanical Thrombectomy With Aspiration

Public Device Record Key

e3d3dd64-2de7-45bd-843c-755e1de85064

Public Version Date

August 12, 2022

Public Version Number

3

DI Record Publish Date

April 18, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-