VIAL ACCESS CANNULA— 510(k) K905664

Substantially Equivalent

Baxter Healthcare Corp

FDA 510(k) clearance K905664 for VIAL ACCESS CANNULA, Substantially Equivalent on 1991-03-15. Applicant: Baxter Healthcare Corp.

Clearance details

Applicant: Baxter Healthcare Corp
Product code: Code FMI
Advisory panel: General Hospital
Date received: 1990-12-18
Decision date: 1991-03-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Round Lake, IL, US

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Adverse events under product code FMI

product code FMI

Death: 28
Injury: 1,517
Malfunction: 23,981
Other: 18
Total: 25,544

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.