The following data is part of a premarket notification filed by Heart Sync Inc. with the FDA for Heart Sync.
Device ID | K131550 |
510k Number | K131550 |
Device Name: | HEART SYNC |
Classification | Automated External Defibrillators (non-wearable) |
Applicant | HEART SYNC INC. 8870 RAVELLO CT Naples, FL 34114 |
Contact | Daniel Kamm |
Correspondent | Daniel Kamm HEART SYNC INC. 8870 RAVELLO CT Naples, FL 34114 |
Product Code | MKJ |
CFR Regulation Number | 870.5310 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-05-29 |
Decision Date | 2013-12-06 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HEART SYNC 85170312 3989284 Live/Registered |
GRAPHIC CONTROLS ACQUISITION CORP. (MICHIGAN) 2010-11-05 |