REDI DRILL DRILL SYSTEM— 510(k) K952609

Substantially Equivalent

Trebay Medical Corp.

FDA 510(k) clearance K952609 for REDI DRILL DRILL SYSTEM, Substantially Equivalent on 1995-07-31. Applicant: Trebay Medical Corp..

Clearance details

Applicant: Trebay Medical Corp.
Product code: Code EQJ
Advisory panel: Ear, Nose, Throat
Date received: 1995-06-07
Decision date: 1995-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code EQJ

product code EQJ

Malfunction: 1,552
Total: 1,552

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.