FDA.report

510(k) K992233

Device
APEX LOCATOR BINGO-1020
Applicant
DENT CORP. RESEARCH & DEVELOPMENT
510(k) number
K992233
Product code
LQY  
Decision
Substantially Equivalent (SESE)
Decision date
1999-11-30
Date received
1999-06-25
Regulation
510(k) Premarket Notification
Classification name
Locator, Root Apex
Medical specialty
510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration   Follow FDA En Español Search FDA   Home Food Drugs Medical Devices
Review panel
Dental
Device class
U
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
DAVID ALBELDA
Address
7-11 S. Broadway White Plains NY US 10601 10601

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

Legacy Summary

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FDA Review

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