The following data is part of a premarket notification filed by Aaron Medical Industries with the FDA for Device, Electrosurgical, Cutting And Coagulation & Accessories.
| Device ID | K950455 |
| 510k Number | K950455 |
| Device Name: | DEVICE, ELECTROSURGICAL, CUTTING AND COAGULATION & ACCESSORIES |
| Classification | Electrode, Electrosurgical |
| Applicant | AARON MEDICAL INDUSTRIES 7100 30TH AVE. NORTH St. Petersburg, FL 33710 |
| Contact | J. Robert Saron |
| Correspondent | J. Robert Saron AARON MEDICAL INDUSTRIES 7100 30TH AVE. NORTH St. Petersburg, FL 33710 |
| Product Code | JOS |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-03 |
| Decision Date | 1995-05-16 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00821925008458 | K950455 | 000 |
| 00821925008083 | K950455 | 000 |