The following data is part of a premarket notification filed by Aaron Medical Industries with the FDA for Nerve Locator/stimulator.
| Device ID | K905045 |
| 510k Number | K905045 |
| Device Name: | NERVE LOCATOR/STIMULATOR |
| Classification | Stimulator, Nerve |
| Applicant | AARON MEDICAL INDUSTRIES 1640 CENTRAL AVE. St. Petersburg, FL 33712 |
| Contact | Robert Saron |
| Correspondent | Robert Saron AARON MEDICAL INDUSTRIES 1640 CENTRAL AVE. St. Petersburg, FL 33712 |
| Product Code | ETN |
| CFR Regulation Number | 874.1820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-11-08 |
| Decision Date | 1991-03-15 |