The following data is part of a premarket notification filed by A-dec, Inc. with the FDA for Synea-hs High Speed-handpiece.
Device ID | K992011 |
510k Number | K992011 |
Device Name: | SYNEA-HS HIGH SPEED-HANDPIECE |
Classification | Handpiece, Air-powered, Dental |
Applicant | A-DEC, INC. 2601 CRESTVIEW DR. Newberg, OR 97132 -9257 |
Contact | Patrick Ridenour |
Correspondent | Patrick Ridenour A-DEC, INC. 2601 CRESTVIEW DR. Newberg, OR 97132 -9257 |
Product Code | EFB |
CFR Regulation Number | 872.4200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-06-15 |
Decision Date | 1999-09-10 |