Medtronic Cryocath Lp
⚠️ Moderate Risk
FEI: 3008389155 • Pointe-Claire, Quebec • CANADA
FEI Number
3008389155
Location
Pointe-Claire, Quebec
Country
CANADAAddress
9000 Rte Transcanadienne, , Pointe-Claire, Quebec, Canada
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/19/2017 | 74OAECATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FIBRILLATION | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 4/19/2017 | 74OAECATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FIBRILLATION | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 4/19/2017 | 74OAECATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FIBRILLATION | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 4/19/2017 | 74OAECATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FIBRILLATION | 508NO 510(K) | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Medtronic Cryocath Lp's FDA import refusal history?
Medtronic Cryocath Lp (FEI: 3008389155) has 4 FDA import refusal record(s) in our database, spanning from 4/19/2017 to 4/19/2017.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Medtronic Cryocath Lp's FEI number is 3008389155.
What types of violations has Medtronic Cryocath Lp received?
Medtronic Cryocath Lp has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Medtronic Cryocath Lp come from?
All FDA import refusal data for Medtronic Cryocath Lp is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.