SATALEC PIEZOTEC

Scaler, Ultrasonic

SPELNA, INC.

The following data is part of a premarket notification filed by Spelna, Inc. with the FDA for Satalec Piezotec.

Pre-market Notification Details

Device IDK852525
510k NumberK852525
Device Name:SATALEC PIEZOTEC
ClassificationScaler, Ultrasonic
Applicant SPELNA, INC. P.O. BOX 3395 Fredericksburg,  VA  22402
ContactRobert E Mcdonnell
CorrespondentRobert E Mcdonnell
SPELNA, INC. P.O. BOX 3395 Fredericksburg,  VA  22402
Product CodeELC  
CFR Regulation Number872.4850 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1985-06-14
Decision Date1986-01-30

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.