ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX— 510(k) K093977

Substantially Equivalent

Chestnut Medical Technologies, Inc.

FDA 510(k) clearance K093977 for ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX, Substantially Equivalent on 2010-04-22. Applicant: Chestnut Medical Technologies, Inc..

Clearance details

Applicant: Chestnut Medical Technologies, Inc.
Product code: Code DQY
Advisory panel: Cardiovascular
Date received: 2009-12-24
Decision date: 2010-04-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQY

product code DQY

Death: 464
Injury: 4,489
Malfunction: 13,721
Other: 2
Total: 18,676

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.