BEECHER 20 GA. PROBE— 510(k) K833800

Substantially Equivalent

Beecher Medical Diagnostic Instrumentation

FDA 510(k) clearance K833800 for BEECHER 20 GA. PROBE, Substantially Equivalent on 1984-01-04. Applicant: Beecher Medical Diagnostic Instrumentation.

Clearance details

Applicant: Beecher Medical Diagnostic Instrumentation
Product code: Code HQC
Advisory panel: Ophthalmic
Date received: 1983-10-31
Decision date: 1984-01-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HQC

product code HQC

Injury: 2,378
Malfunction: 8,768
Total: 11,146

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.