FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ANGIOJET SOLENT OMNI THROMBECTOMY SET
K Number: K111182
·
Decision May 24, 2011
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
91
Applicant Total
105
Review Days
27
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Basic Information
- Device Name
- ANGIOJET SOLENT OMNI THROMBECTOMY SET
- K Number
- K111182
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.5150
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medrad, Inc.
- Date Received
- April 27, 2011
- Decision Date
- May 24, 2011
- Product Code
- QEZ
- 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 |
|---|---|---|---|
| QEZ | Aspiration Thrombectomy Catheter | FDA class 2 | Cardiovascular |
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