SIDEPORT PINCH CLAMP DEVICE— 510(k) K010888

Substantially Equivalent

Medivice Systems, Ltd.

FDA 510(k) clearance K010888 for SIDEPORT PINCH CLAMP DEVICE, Substantially Equivalent on 2001-06-27. Applicant: Medivice Systems, Ltd..

Clearance details

Applicant: Medivice Systems, Ltd.
Product code: Code FPA
Advisory panel: General Hospital
Date received: 2001-03-23
Decision date: 2001-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kfar Saba, IL

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Adverse events under product code FPA

product code FPA

Death: 95
Injury: 14,421
Malfunction: 125,815
Other: 30
Total: 140,361

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.