X-TIP INTRAOSSEOUS PERFORATOR

Needle, Dental

SCHIFF & CO.

The following data is part of a premarket notification filed by Schiff & Co. with the FDA for X-tip Intraosseous Perforator.

Pre-market Notification Details

Device IDK990511
510k NumberK990511
Device Name:X-TIP INTRAOSSEOUS PERFORATOR
ClassificationNeedle, Dental
Applicant SCHIFF & CO. 1129 BLOOMFIELD AVE. West Caldwell,  NJ  07006
ContactRobert Schiff
CorrespondentRobert Schiff
SCHIFF & CO. 1129 BLOOMFIELD AVE. West Caldwell,  NJ  07006
Product CodeDZM  
CFR Regulation Number872.4730 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1999-02-18
Decision Date1999-04-27

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