CORFLO ANTI IV ENTERAL FEEDING TUBE— 510(k) K083210
Substantially EquivalentCorpak Medsystems
FDA 510(k) clearance K083210 for CORFLO ANTI IV ENTERAL FEEDING TUBE, Substantially Equivalent on 2008-12-29. 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
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wheeling, IL, US
Recent devices under product code FPD
view allMore clearances from Corpak Medsystems
view allAdverse events under product code FPD
product code FPD- Death
- 6
- Other
- 1
- Total
- 7
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 →
Recalls naming K083210
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K083210.
Data sourced from openFDA. This site is unofficial and independent of the FDA.