ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER— 510(k) K984189
Substantially EquivalentMaxxim Medical
FDA 510(k) clearance K984189 for ARGON MULTI-LUMEN CENTRAL VENOUS CATHETER, Substantially Equivalent on 1999-05-05. Applicant: Maxxim Medical. Device class: 2.
Clearance details
- Applicant
- Maxxim Medical
- Product code
- Code FOZ
- Device class
- Class 2
- Regulation
- 21 CFR 880.5200
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Athens, TX, US
Recent devices under product code FOZ
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- K002847 — INTRODUCER WITH DISTAL RADIOPAQUE MARKER BAND, MODEL OR-4926XX
- K010297 — SENSICARE SYNTHETIC POWDER FREE SURGICAL GLOVES (POLY ISOPRENE)
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, through . 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.