FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
XCATH
K Number: K133296
·
Decision Feb 14, 2014
Classifications
1
FEI Numbers
268
Registration Numbers
268
Same Product Code
682
Applicant Total
3
Review Days
112
Basic Information
- Device Name
- XCATH
- K Number
- K133296
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- ALSEAL
- Date Received
- October 25, 2013
- Decision Date
- February 14, 2014
- Product Code
- DYB
- 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 |
|---|---|---|---|
| DYB | Introducer, Catheter | FDA class 2 | Cardiovascular |
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