The following data is part of a premarket notification filed by Spelna, Inc. with the FDA for Satalec Piezotec.
Device ID | K852525 |
510k Number | K852525 |
Device Name: | SATALEC PIEZOTEC |
Classification | Scaler, Ultrasonic |
Applicant | SPELNA, INC. P.O. BOX 3395 Fredericksburg, VA 22402 |
Contact | Robert E Mcdonnell |
Correspondent | Robert E Mcdonnell SPELNA, INC. P.O. BOX 3395 Fredericksburg, VA 22402 |
Product Code | ELC |
CFR Regulation Number | 872.4850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-06-14 |
Decision Date | 1986-01-30 |