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 |