The following data is part of a premarket notification filed by Medic Nrg Ltd. with the FDA for Apex Nrg.
| Device ID | K032743 |
| 510k Number | K032743 |
| Device Name: | APEX NRG |
| Classification | Locator, Root Apex |
| Applicant | MEDIC NRG LTD. POB 367 Ramat Hasharon, IL 47103 |
| Contact | Adi Ickowicz |
| Correspondent | Adi Ickowicz MEDIC NRG LTD. POB 367 Ramat Hasharon, IL 47103 |
| 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 | 2003-09-04 |
| Decision Date | 2004-03-15 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| H834017231800 | K032743 | 000 |