REVEAL DX INSERTABLE CARDIAC MONITOR, REVEAL PATIENT ASSISTANT, MODEL(S) 9528,9538— 510(k) K071655

Substantially Equivalent

Medtronic, Inc.

FDA 510(k) clearance K071655 for REVEAL DX INSERTABLE CARDIAC MONITOR, REVEAL PATIENT ASSISTANT, MODEL(S) 9528,9538, Substantially Equivalent on 2007-11-21. Applicant: Medtronic, Inc..

Clearance details

Applicant: Medtronic, Inc.
Product code: Code DSI
Advisory panel: Cardiovascular
Date received: 2007-06-18
Decision date: 2007-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mounds View, MN, US

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Adverse events under product code DSI

product code DSI

Death: 170
Injury: 729
Malfunction: 10,680
Total: 11,579

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.