PARADIGM QUICK-SET INFUSION SET— 510(k) K011071
Substantially EquivalentMaersk Medical A/S
FDA 510(k) clearance K011071 for PARADIGM QUICK-SET INFUSION SET, Substantially Equivalent on 2001-06-07. Applicant: Maersk Medical A/S. Device class: 2.
Clearance details
- Applicant
- Maersk Medical A/S
- 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
- Northridge, CA, US
Recent devices under product code FPA
view all- K254123 — Ecomed Disposable Administration Sets
- K261530 — iiSure Infusion Set
- K252543 — AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)
- K251375 — PuraCath Firefly Needleless Connector IT (9005)
- K251257 — nSet+ Stabilization Set [6426733] +2 more
More clearances from Maersk Medical A/S
view all- K002138 — PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380
- K990110 — DISPOSABLE ECG MONITORING ELECTRODES, MODEL 4110, 4140
- K990111 — DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4520, 4535, 4570
- K990112 — DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4060, 4610
- K990113 — DISPOSABLE ECG MONITORING ELECTRODES, MODELS 4500,4530, 4533, 4539, 4540, AND 4560
Adverse 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 K011071
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 K011071.
Data sourced from openFDA. This site is unofficial and independent of the FDA.