NAMIC CONTRAST & FLUID DELIVERY SPIKES(VARIOUS)— 510(k) K852140
Substantially EquivalentNorth American Instrument Corp.
FDA 510(k) clearance K852140 for NAMIC CONTRAST & FLUID DELIVERY SPIKES(VARIOUS), Substantially Equivalent on 1985-05-30. Applicant: North American Instrument Corp.. Device class: 2.
Clearance details
- Applicant
- North American Instrument Corp.
- Product code
- Code FPA
- Device class
- Class 2
- Regulation
- 21 CFR 880.5440
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- NY, US
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More clearances from North American Instrument Corp.
view allAdverse events under product code FPA
product code FPA- Death
- 95
- Injury
- 14,421
- Malfunction
- 125,815
- Other
- 30
- Total
- 140,361
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 K852140
K-number listed on FDA's recall record- Z-0764-2025 — Medline Fluid Delivery Set with Drip Chamber: 1) FDS,135,CHMN,W/F,MLL,RC(2),PG, Item Number 99000069; 2) FDS,135,NV,MICRO-CHAMBER,W/FILTER,BLUE, Item Number 949000222; 3) FDS,135,NV,MICRO-CHAMBER,W/FILTER,GREEN, Item Number 949000224; 4) FDS,135,NV,MICRO-CHAMBER,W/FILTER,RED, Item Number 949000221; 5) FDS,135,NV,MICRO-CHAMBER,W/FILTER,YELLOW, Item Number 949000223
- Z-1807-2024 — Namic FLUID DELIVERY SET, REF 91300040
- Z-1853-2017 — NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K852140.
Data sourced from openFDA. This site is unofficial and independent of the FDA.