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 |
00887482177631 | K020579 | 000 |
00887482177655 | K020579 | 000 |
00887482181492 | K020579 | 000 |
20884524000128 | 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 |
00887482177617 | K020579 | 000 |