CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1030AIV-LB-S— 510(k) K083776

Name: FDA 510(k) clearance K083776
Creator: U.S. Food and Drug Administration
Published: 2009-03-05

Substantially Equivalent

Corpak Medsystems

FDA 510(k) clearance K083776 for CORFLO ANTI IV ENTERAL FEEDING SET, MODEL: 20-1030AIV-LB-S, Substantially Equivalent on 2009-03-05. Applicant: Corpak Medsystems. Device class: 2.

Clearance details

Applicant: Corpak Medsystems
Product code: Code FPD
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 2008-12-19
Decision date: 2009-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheeling, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FPD

view all

K243361 — Nutrifit2024-12-19
K180236 — VR Medical Feeding Tube and Enteral Feeding Extension Set (EFES)2019-01-18
K131590 — INNERSENSE ESOPHAGEAL TEMPERATURE PROBE / FEEDING TUBE2013-10-23
K120815 — INNERSENSE ESOPHAGEAL TEMPERATURE/FEEDING TUBE2013-03-06
K121105 — NUTRISAFE 2 FEEDING TUBE2012-12-18

More clearances from Corpak Medsystems

view all

K142012 — FARRELL VALVE SYSTEM WITH EQUILIBRIUM TECHNOLOGY AND ENFIT ENTERAL CONNECTORS2014-11-20
K133599 — CORGRIP2014-03-26
K131532 — ELECTROMAGNETIC TRANSMITTING STYLET2013-08-12
K113351 — CORTRAK ENTERAL ACCESS DEVICE2012-01-10
K100365 — FARRELL VALVE WITH CORFLO ANTI-IV CONNECTORS MODEL 20-4300AIV2010-05-20

Adverse events under product code FPD

product code FPD

Death: 6
Other: 1
Total: 7

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.