CONTINUOUS FLUSH DEVICE— 510(k) K792141

Substantially Equivalent

Pharmaseal Div., Baxter Healthcare Corp.

FDA 510(k) clearance K792141 for CONTINUOUS FLUSH DEVICE, Substantially Equivalent on 1979-12-05. Applicant: Pharmaseal Div., Baxter Healthcare Corp..

Clearance details

Applicant: Pharmaseal Div., Baxter Healthcare Corp.
Product code: Code KRA
Advisory panel: Cardiovascular
Date received: 1979-10-22
Decision date: 1979-12-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code KRA

product code KRA

Death: 234
Injury: 1,029
Malfunction: 3,012
Other: 2
Total: 4,277

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.