BLOOD TUBING SET— 510(k) K884243

Name: FDA 510(k) clearance K884243
Creator: U.S. Food and Drug Administration
Published: 1988-12-08

Substantially Equivalent

Mediflex Intl.

FDA 510(k) clearance K884243 for BLOOD TUBING SET, Substantially Equivalent on 1988-12-08. Applicant: Mediflex Intl.. Device class: 2.

Clearance details

Applicant: Mediflex Intl.
Product code: Code FJK
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1988-10-11
Decision date: 1988-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairfield, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FJK

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K252423 — NovaLine Tubing Set for Hemodialysis (BL 124)2026-05-15
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K251442 — TIANYI Extracorporeal Blood Tubing Set (TY-NDEO-A1)2025-10-02
K243607 — Moda-flx Hemodialysis System Cartridge (102121-001 )2024-12-20
K213992 — CombiSet Hemodialysis Blood Tubing Set2023-05-31

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K915140 — PRIMARY DRESSING TRAY1992-02-11
K900841 — HEMODIALYSIS TRANSDUCER PROTECTOR1990-05-15
K891077 — MEDIVERSE PARENTERAL NUTRITION BAG1989-05-24
K863496 — MEDIFLEX TRANSDUCER PROTECTOR1986-09-23
K855039 — MEDIFLEX INJECTION CAP1986-01-24

Adverse events under product code FJK

product code FJK

Death: 52
Malfunction: 3,430
Total: 3,482

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.