APEX LOCATOR BINGO-1020— 510(k) K992233

Name: FDA 510(k) clearance K992233
Creator: U.S. Food and Drug Administration
Published: 1999-11-30

Substantially Equivalent

Dent Corp. Research & Development

FDA 510(k) clearance K992233 for APEX LOCATOR BINGO-1020, Substantially Equivalent on 1999-11-30. Applicant: Dent Corp. Research & Development. Device class: Unclassified.

Clearance details

Applicant: Dent Corp. Research & Development
Product code: Code LQY
Device class: Unclassified
Advisory panel: Unknown
Date received: 1999-06-25
Decision date: 1999-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: White Plains, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LQY

product code LQY

Malfunction: 504
Total: 504

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.