SURGITEK FOERSTER FACE LIFT DRAIN— 510(k) K800331

Substantially Equivalent

Medical Engineering Corp.

FDA 510(k) clearance K800331 for SURGITEK FOERSTER FACE LIFT DRAIN, Substantially Equivalent on 1980-03-05. Applicant: Medical Engineering Corp..

Clearance details

Applicant: Medical Engineering Corp.
Product code: Code GCY
Advisory panel: General, Plastic Surgery
Date received: 1980-02-13
Decision date: 1980-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code GCY

product code GCY

Malfunction: 786
Other: 1
Total: 787

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.