MODIFIED BLOOD RECIPIENT SET— 510(k) K993120

Substantially Equivalent

Baxter Healthcare Corp

FDA 510(k) clearance K993120 for MODIFIED BLOOD RECIPIENT SET, Substantially Equivalent on 1999-11-17. Applicant: Baxter Healthcare Corp.

Clearance details

Applicant: Baxter Healthcare Corp
Product code: Code BRZ
Advisory panel: General Hospital
Date received: 1999-09-20
Decision date: 1999-11-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Round Lake, IL, US

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Adverse events under product code BRZ

product code BRZ

Malfunction: 458
Total: 458

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.