VIT ENHANCER— 510(k) K992943

Substantially Equivalent

Medical Instrument Development Laboratories, Inc.

FDA 510(k) clearance K992943 for VIT ENHANCER, Substantially Equivalent on 1999-12-10. Applicant: Medical Instrument Development Laboratories, Inc..

Clearance details

Applicant: Medical Instrument Development Laboratories, Inc.
Product code: Code HQE
Advisory panel: Ophthalmic
Date received: 1999-08-31
Decision date: 1999-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Leandro, CA, US

Download summary PDF View on FDA.gov ↗

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.