The following data is part of a premarket notification filed by Rhythmia Medical, Inc with the FDA for Rhythmia Mapping Catheter.
| Device ID | K122461 |
| 510k Number | K122461 |
| Device Name: | RHYTHMIA MAPPING CATHETER |
| Classification | Catheter, Electrode Recording, Or Probe, Electrode Recording |
| Applicant | RHYTHMIA MEDICAL, INC 111 SOUTH BEDFORD ST SUITE 205 Burlington, MA 01803 |
| Contact | Leon Amariglio |
| Correspondent | Leon Amariglio RHYTHMIA MEDICAL, INC 111 SOUTH BEDFORD ST SUITE 205 Burlington, MA 01803 |
| Product Code | DRF |
| CFR Regulation Number | 870.1220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-08-13 |
| Decision Date | 2013-04-18 |
| Summary: | summary |