VISITEC PRECISE-POINT— 510(k) K942234

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K942234 for VISITEC PRECISE-POINT, Substantially Equivalent on 1994-07-12. Applicant: Visitec Co..

Clearance details

Applicant: Visitec Co.
Product code: Code GAP
Advisory panel: General, Plastic Surgery
Date received: 1994-05-09
Decision date: 1994-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sarasota, FL, US

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Adverse events under product code GAP

product code GAP

Death: 3
Injury: 491
Malfunction: 2,253
Total: 2,747

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.