FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HEMASHIELD GOLD WOVEN DOUBLE VELOUR VASCULAR GRAFT - BRANCH GRAFT
K Number: K012952
·
Decision Oct 2, 2001
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
187
Applicant Total
5
Review Days
28
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Basic Information
- Device Name
- HEMASHIELD GOLD WOVEN DOUBLE VELOUR VASCULAR GRAFT - BRANCH GRAFT
- K Number
- K012952
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.3450
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Boston Scientific/Medi-Tech
- Date Received
- September 4, 2001
- Decision Date
- October 2, 2001
- Product Code
- DSY
- 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 |
|---|---|---|---|
| DSY | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter | FDA class 2 | Cardiovascular |
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Other Clearances by Boston Scientific/Medi-Tech
| K Number | Device Name | ||
|---|---|---|---|
| K023870 | FLEXIMA BILIARY CATHETER | Dec 20, 2002 | Substantially Equivalent |
| K020012 | MODIFICATION TO RENEGADE FIBER BRAIDED MICROCATHETER | Jan 29, 2002 | Substantially Equivalent |
| K012948 | MODIFICATION TO VAXCEL DIALYSIS CATHETER | Oct 3, 2001 | Substantially Equivalent |
| K011664 | IMAGER II ANGIOGRAPHIC CATHETER | Sep 7, 2001 | Substantially Equivalent |