7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM— 510(k) K880776
Substantially EquivalentMedsurg Industries, Inc.
FDA 510(k) clearance K880776 for 7 FR. TRIPLE LUMEN CENTRAL VEIN CATHETERI. SYSTEM, Substantially Equivalent on 1988-05-02. Applicant: Medsurg Industries, Inc.. Device class: 2.
Clearance details
- Applicant
- Medsurg Industries, Inc.
- Product code
- Code DQR
- Device class
- Class 2
- Regulation
- 21 CFR 870.1300
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Herndon, VA, US
Recent devices under product code DQR
view all- K131446 — INTEGRA JARIT HEPARIN CANNULAS, INJECTORS, AND NEEDLES
- K073559 — 18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA II
- K051655 — ANGIODYNAMICS, INC., MICRO ACCESS KITS
- K030398 — CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221
- K960098 — RMI INTERNAL MAMMARY ARTERY CANNULA
More clearances from Medsurg Industries, Inc.
view allAdverse events under product code DQR
product code DQR- Death
- 2
- Total
- 2
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.