ULTRASONIC DENTAL PROPHYLAXIS DEVICE

Scaler, Ultrasonic

CAVITRON CORP.

The following data is part of a premarket notification filed by Cavitron Corp. with the FDA for Ultrasonic Dental Prophylaxis Device.

Pre-market Notification Details

Device IDK760805
510k NumberK760805
Device Name:ULTRASONIC DENTAL PROPHYLAXIS DEVICE
ClassificationScaler, Ultrasonic
Applicant CAVITRON CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeELC  
CFR Regulation Number872.4850 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1976-10-12
Decision Date1976-10-21

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