INLINE AUTOTRANSFUSION SYSTEM— 510(k) K890171

Substantially Equivalent

Conmedcorp

FDA 510(k) clearance K890171 for INLINE AUTOTRANSFUSION SYSTEM, Substantially Equivalent on 1989-06-15. Applicant: Conmedcorp.

Clearance details

Applicant: Conmedcorp
Product code: Code CAC
Advisory panel: Anesthesiology
Date received: 1989-01-17
Decision date: 1989-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Utica, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code CAC

product code CAC

Death: 11
Malfunction: 477
Total: 488

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.