PROCELLERA— 510(k) K130350

Substantially Equivalent

Vomaris Innovations, Inc.

FDA 510(k) clearance K130350 for PROCELLERA, Substantially Equivalent on 2013-07-02. Applicant: Vomaris Innovations, Inc..

Clearance details

Applicant: Vomaris Innovations, Inc.
Product code: Code FRO
Advisory panel: Unknown
Date received: 2013-02-12
Decision date: 2013-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chandler, AZ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FRO

product code FRO

Death: 30
Injury: 653
Malfunction: 479
Other: 11
Total: 1,173

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.