BLOOD PORT CAP, DIALYSATE PORT CAP, RED HARD PLASTIC— 510(k) K961040

Substantially Equivalent

Dayspring Medical, Inc.

FDA 510(k) clearance K961040 for BLOOD PORT CAP, DIALYSATE PORT CAP, RED HARD PLASTIC, Substantially Equivalent on 1996-06-11. Applicant: Dayspring Medical, Inc..

Clearance details

Applicant: Dayspring Medical, Inc.
Product code: Code FJI
Advisory panel: Gastroenterology, Urology
Date received: 1996-03-14
Decision date: 1996-06-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boulder, CO, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FJI

product code FJI

Death: 2
Total: 2

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.