The following data is part of a premarket notification filed by Satelec with the FDA for Suprasson P Max.
Device ID | K942139 |
510k Number | K942139 |
Device Name: | SUPRASSON P MAX |
Classification | Scaler, Ultrasonic |
Applicant | SATELEC Z.I. DU PHARE, B.P. 216 17, AVENUE GUSTAVE EIFFEL Merignac Cedex, FR 33708 |
Contact | Pascal Dupeyron |
Correspondent | Pascal Dupeyron SATELEC Z.I. DU PHARE, B.P. 216 17, AVENUE GUSTAVE EIFFEL Merignac Cedex, FR 33708 |
Product Code | ELC |
CFR Regulation Number | 872.4850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-05-03 |
Decision Date | 1995-09-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SUPRASSON P MAX 74487055 1950071 Live/Registered |
SOCIETE POUR LA CONCEPTION DES APPLICATIONS DES TECHNIQUES ELECTRONIQUES, SATELEC 1994-02-07 |