REVIVE INTERMEDIATE CATHETER (REVIVE IC)— 510(k) K112828

Substantially Equivalent

Codman & Shurtleff, Inc.

FDA 510(k) clearance K112828 for REVIVE INTERMEDIATE CATHETER (REVIVE IC), Substantially Equivalent on 2011-10-25. Applicant: Codman & Shurtleff, Inc..

Clearance details

Applicant: Codman & Shurtleff, Inc.
Product code: Code DQY
Advisory panel: Cardiovascular
Date received: 2011-09-28
Decision date: 2011-10-25
Decision: Substantially Equivalent
Clearance type: Special
Location: Raynham, MA, US

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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.