The following data is part of a premarket notification filed by Medicnrg Ltd. with the FDA for Apexnrg-blue Electronic Apex Locator.
Device ID | K071133 |
510k Number | K071133 |
Device Name: | APEXNRG-BLUE ELECTRONIC APEX LOCATOR |
Classification | Locator, Root Apex |
Applicant | MEDICNRG LTD. 291 HILLSIDE AVE. Somerset, MA 02726 |
Contact | George J Hattub |
Correspondent | George J 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 | 2007-04-23 |
Decision Date | 2007-09-21 |
Summary: | summary |