The following data is part of a premarket notification filed by Medicnrg Ltd. with the FDA for Apexnrg Rider.
| Device ID | K101177 |
| 510k Number | K101177 |
| Device Name: | APEXNRG RIDER |
| Classification | Locator, Root Apex |
| Applicant | MEDICNRG LTD. 291 HILLSIDE AVE. Somerset, MA 02726 |
| Contact | George Hattub |
| Correspondent | George Hattub MEDICNRG LTD. 291 HILLSIDE AVE. Somerset, MA 02726 |
| Product Code | LQY |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-04-27 |
| Decision Date | 2010-10-08 |
| Summary: | summary |