Navigator Aesthetic Delivery System— 510(k) K151255

Substantially Equivalent

Carticept Medical, Inc.

FDA 510(k) clearance K151255 for Navigator Aesthetic Delivery System, Substantially Equivalent on 2015-12-30. Applicant: Carticept Medical, Inc..

Clearance details

Applicant: Carticept Medical, Inc.
Product code: Code FRN
Advisory panel: General Hospital
Date received: 2015-05-12
Decision date: 2015-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alpharetta, GA, US

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Adverse events under product code FRN

product code FRN

Death: 540
Injury: 6,178
Malfunction: 1,464,165
Other: 52
Total: 1,470,935

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.