FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Ablacath Mapping Catheter
K Number: K223666
·
Decision Mar 17, 2023
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
33
Applicant Total
3
Review Days
100
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Basic Information
- Device Name
- Ablacath Mapping Catheter
- K Number
- K223666
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1220
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ablacon, Inc.
- Date Received
- December 7, 2022
- Decision Date
- March 17, 2023
- Product Code
- MTD
- 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 |
|---|---|---|---|
| MTD | Catheter, Intracardiac Mapping, High-Density Array | FDA class 2 | Cardiovascular |
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