circul pro Ring— 510(k) K221361

Substantially Equivalent

Bodimetrics, LLC

FDA 510(k) clearance K221361 for circul pro Ring, Substantially Equivalent on 2023-08-29. Applicant: Bodimetrics, LLC.

Clearance details

Applicant: Bodimetrics, LLC
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 2022-05-11
Decision date: 2023-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Manhattan Beach, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DQA

product code DQA

Death: 66
Malfunction: 2,867
Other: 1
Total: 2,934

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.