The following data is part of a premarket notification filed by Sodem Systems with the FDA for Sodem High Speed System (electric) (ear, Nose, And Throat).
Device ID | K012456 |
510k Number | K012456 |
Device Name: | SODEM HIGH SPEED SYSTEM (ELECTRIC) (EAR, NOSE, AND THROAT) |
Classification | Drill, Surgical, Ent (electric Or Pneumatic) Including Handpiece |
Applicant | SODEM SYSTEMS 110 CH. DU PONT DU CENTENAIRE Geneva, CH Ch-1228 |
Contact | Carole Burnier |
Correspondent | Carole Burnier SODEM SYSTEMS 110 CH. DU PONT DU CENTENAIRE Geneva, CH Ch-1228 |
Product Code | ERL |
CFR Regulation Number | 874.4250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-08-01 |
Decision Date | 2001-09-21 |
Summary: | summary |