PROTECTIV JELCO SAFETY I.V. CATHETER, MODEL 3600 SERIES— 510(k) K041345

Name: FDA 510(k) clearance K041345
Creator: U.S. Food and Drug Administration
Published: 2004-07-22

Substantially Equivalent

Medix, Inc.

FDA 510(k) clearance K041345 for PROTECTIV JELCO SAFETY I.V. CATHETER, MODEL 3600 SERIES, Substantially Equivalent on 2004-07-22. Applicant: Medix, Inc.. Device class: 2.

Clearance details

Applicant: Medix, Inc.
Product code: Code FOZ
Device class: Class 2
Regulation: 21 CFR 880.5200
Advisory panel: General Hospital
Date received: 2004-05-20
Decision date: 2004-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dublin, OH, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FOZ

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K260432 — Ruby Intravascular Catheter2026-09-02
K260165 — Unimpregnated Central Venous Catheter2026-08-10
K261041 — ClearSafe Closed System2026-07-10
K260539 — MedSource QuickSafe Safety IV Catheter; MedSource PurSafe Safety IV Catheter2026-07-09
K253235 — Introcan Safety® Deep Access XL IV Catheter2026-05-15

Adverse events under product code FOZ

product code FOZ

Death: 38
Injury: 2,290
Malfunction: 25,858
Other: 11
Total: 28,197

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.