THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE— 510(k) K930842

Substantially Equivalent

Grieshaber & Co.

FDA 510(k) clearance K930842 for THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE, Substantially Equivalent on 1994-05-03. Applicant: Grieshaber & Co..

Clearance details

Applicant: Grieshaber & Co.
Product code: Code HQE
Advisory panel: Ophthalmic
Date received: 1993-02-17
Decision date: 1994-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kennesaw, GA, US

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Adverse events under product code HQE

product code HQE

Injury: 156
Malfunction: 565
Total: 721

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.