Catalog Number

18-1342

Brand Name

HeartLight

Version/Model Number

18-1342

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

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

P150026

Product Code

OAE

Product Code Name

Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation

Public Device Record Key

70f44d2c-d4ed-48c9-8cda-4d88faaa68e5

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

June 15, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-