The following data is part of a premarket notification filed by E.m.s. Electro Medical Systems S.a. with the FDA for Air-flow Handy 3.0.
Device ID | K132478 |
510k Number | K132478 |
Device Name: | AIR-FLOW HANDY 3.0 |
Classification | Handpiece, Air-powered, Dental |
Applicant | E.M.S. ELECTRO MEDICAL SYSTEMS S.A. 62 FOREST ST., STE 300 Marlborough, MA 01752 |
Contact | Cynthia J Nolte |
Correspondent | Cynthia J Nolte E.M.S. ELECTRO MEDICAL SYSTEMS S.A. 62 FOREST ST., STE 300 Marlborough, MA 01752 |
Product Code | EFB |
CFR Regulation Number | 872.4200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-08-08 |
Decision Date | 2014-04-11 |
Summary: | summary |