FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
OSTIAL PRO STENT POSITIONING SYSTEM
K Number: K062192
·
Decision May 24, 2007
Classifications
1
FEI Numbers
252
Registration Numbers
253
Same Product Code
751
Applicant Total
1
Review Days
297
Basic Information
- Device Name
- OSTIAL PRO STENT POSITIONING SYSTEM
- K Number
- K062192
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1330
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- OSTIAL SOLUTIONS, LLC
- Date Received
- July 31, 2006
- Decision Date
- May 24, 2007
- Product Code
- DQX
- 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 |
|---|---|---|---|
| DQX | Wire, Guide, Catheter | FDA class 2 | Cardiovascular |
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