The following data is part of a premarket notification filed by Aaron Medical Industries with the FDA for Aaron Arthroscopy Electrode, Catalog Numbers Ar00, Ar01, Ar02, And Ar03.
| Device ID | K020579 |
| 510k Number | K020579 |
| Device Name: | AARON ARTHROSCOPY ELECTRODE, CATALOG NUMBERS AR00, AR01, AR02, AND AR03 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | AARON MEDICAL INDUSTRIES 7100 30TH AVE. NORTH St. Petersburg, FL 33710 -2902 |
| Contact | Richard A Kozloff |
| Correspondent | Richard A Kozloff AARON MEDICAL INDUSTRIES 7100 30TH AVE. NORTH St. Petersburg, FL 33710 -2902 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-02-21 |
| Decision Date | 2002-05-13 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 50749756277339 | K020579 | 000 |
| 20884524000135 | K020579 | 000 |
| 20884524000142 | K020579 | 000 |
| 20884524000470 | K020579 | 000 |
| 20884524000487 | K020579 | 000 |
| 20884524000036 | K020579 | 000 |
| 50749756267392 | K020579 | 000 |
| 50749756277278 | K020579 | 000 |
| 50749756277322 | K020579 | 000 |
| 20884524000128 | K020579 | 000 |