FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFICATION TO: EXPORT CATHETER
K Number: K050139
·
Decision Mar 22, 2005
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
91
Applicant Total
475
Review Days
60
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Basic Information
- Device Name
- MODIFICATION TO: EXPORT CATHETER
- K Number
- K050139
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.5150
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Medtronic Vascular
- Date Received
- January 21, 2005
- Decision Date
- March 22, 2005
- 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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