FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Prestige Coil System
K Number: K220699
·
Decision Apr 8, 2022
Classifications
1
FEI Numbers
103
Registration Numbers
103
Same Product Code
128
Applicant Total
1
Review Days
29
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Basic Information
- Device Name
- Prestige Coil System
- K Number
- K220699
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.3300
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Bait USA, LLC
- Date Received
- March 10, 2022
- Decision Date
- April 8, 2022
- Product Code
- KRD
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KRD | Device, Vascular, For Promoting Embolization | FDA class 2 | Cardiovascular |
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