VASOSTAT HEMOSTASIS DEVICE— 510(k) K123041

Substantially Equivalent

Forge Medical, Inc.

FDA 510(k) clearance K123041 for VASOSTAT HEMOSTASIS DEVICE, Substantially Equivalent on 2013-05-29. Applicant: Forge Medical, Inc..

Clearance details

Applicant: Forge Medical, Inc.
Product code: Code DXC
Advisory panel: Cardiovascular
Date received: 2012-09-28
Decision date: 2013-05-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayne, NJ, US

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Adverse events under product code DXC

product code DXC

Death: 14
Injury: 442
Malfunction: 2,209
Other: 1
Total: 2,666

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.