STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR— 510(k) K885247

Substantially Equivalent

Baxter Healthcare Corp

FDA 510(k) clearance K885247 for STANDARD, TUOHY BORST & DUAL VALVE Y-CONNECTOR, Substantially Equivalent on 1989-03-10. Applicant: Baxter Healthcare Corp.

Clearance details

Applicant: Baxter Healthcare Corp
Product code: Code LIT
Advisory panel: Cardiovascular
Date received: 1988-12-22
Decision date: 1989-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Ana, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LIT

product code LIT

Death: 27
Injury: 1,256
Malfunction: 12,127
Total: 13,410

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.