Surdial DX Hemodialysis System— 510(k) K182940
Substantially EquivalentNipro Medical Corporation
FDA 510(k) clearance K182940 for Surdial DX Hemodialysis System, Substantially Equivalent on 2019-07-19. Applicant: Nipro Medical Corporation. Device class: 2.
Clearance details
- Applicant
- Nipro Medical Corporation
- Product code
- Code KDI
- Device class
- Class 2
- Regulation
- 21 CFR 876.5860
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
Recent devices under product code KDI
view allMore clearances from Nipro Medical Corporation
view allAdverse events under product code KDI
product code KDI- Death
- 352
- Injury
- 1,474
- Malfunction
- 12,534
- Other
- 4
- Total
- 14,364
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 K182940
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 K182940.
Data sourced from openFDA. This site is unofficial and independent of the FDA.