HORIZON 2000/S 266-XXX-XXX— 510(k) K880595

Substantially Equivalent

Mennen Medical, Inc.

FDA 510(k) clearance K880595 for HORIZON 2000/S 266-XXX-XXX, Substantially Equivalent on 1988-05-06. Applicant: Mennen Medical, Inc..

Clearance details

Applicant: Mennen Medical, Inc.
Product code: Code DPS
Advisory panel: Cardiovascular
Date received: 1988-02-11
Decision date: 1988-05-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clarence, NY, US

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Adverse events under product code DPS

product code DPS

Death: 7
Total: 7

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.