FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STEERABLE GUIDE CATHETER
K Number: K112239
·
Decision Aug 31, 2011
Classifications
1
FEI Numbers
46
Registration Numbers
47
Same Product Code
40
Applicant Total
30
Review Days
27
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Basic Information
- Device Name
- STEERABLE GUIDE CATHETER
- K Number
- K112239
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.1280
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Abbott Vascular
- Date Received
- August 4, 2011
- Decision Date
- August 31, 2011
- Product Code
- DRA
- 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 |
|---|---|---|---|
| DRA | Catheter, Steerable | FDA class 2 | Cardiovascular |
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