The following data is part of a premarket notification filed by Access Point Technologies Ep, Inc. with the FDA for Map-it Diagnostic Mapping Catheters.
| Device ID | K160390 |
| 510k Number | K160390 |
| Device Name: | Map-it Diagnostic Mapping Catheters |
| Classification | Catheter, Electrode Recording, Or Probe, Electrode Recording |
| Applicant | ACCESS POINT TECHNOLOGIES EP, INC. 12560 LOCATED AT FLETCHER LANE SUITE 3 Rogers, MN 55374 |
| Contact | Sean Carroll |
| Correspondent | Laurie Lewandowski HONKANEN CONSULTING, INC. 738 SADDLE WOOD DRIVE Eagan, MN 55123 |
| Product Code | DRF |
| CFR Regulation Number | 870.1220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-02-11 |
| Decision Date | 2016-04-11 |
| Summary: | summary |