STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115A & 1100C-230A— 510(k) K042909

Substantially Equivalent

Stellartech Research Corp.

FDA 510(k) clearance K042909 for STELLARTECH COAGULATION SYSTEM, MODELS 1100C-115A & 1100C-230A, Substantially Equivalent on 2004-11-12. Applicant: Stellartech Research Corp..

Clearance details

Applicant: Stellartech Research Corp.
Product code: Code GEI
Advisory panel: General, Plastic Surgery
Date received: 2004-10-21
Decision date: 2004-11-12
Decision: Substantially Equivalent
Clearance type: Special
Location: Sunnyvale, CA, US

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Adverse events under product code GEI

product code GEI

Death: 133
Injury: 7,585
Malfunction: 35,808
Other: 44
Total: 43,570

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.