IPULSE, MODEL I400— 510(k) K080406

Substantially Equivalent

Cyden Limited

FDA 510(k) clearance K080406 for IPULSE, MODEL I400, Substantially Equivalent on 2008-03-10. Applicant: Cyden Limited.

Clearance details

Applicant: Cyden Limited
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2008-02-14
Decision date: 2008-03-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Swansea, Wales, GB

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.