PRO-VIT— 510(k) K950799

Substantially Equivalent

M. Imonti and Associates Inc.,

FDA 510(k) clearance K950799 for PRO-VIT, Substantially Equivalent on 1995-04-28. Applicant: M. Imonti and Associates Inc.,.

Clearance details

Applicant: M. Imonti and Associates Inc.,
Product code: Code HQE
Advisory panel: Ophthalmic
Date received: 1995-02-21
Decision date: 1995-04-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Juan Capistrano, CA, 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.