FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GELBISH VASCULAR DILATOR
K Number: K012256
·
Decision Dec 20, 2001
Classifications
1
FEI Numbers
100
Registration Numbers
100
Same Product Code
103
Applicant Total
3
Review Days
155
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Basic Information
- Device Name
- GELBISH VASCULAR DILATOR
- K Number
- K012256
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1310
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Vascumetrix, LLC
- Date Received
- July 18, 2001
- Decision Date
- December 20, 2001
- Product Code
- DRE
- 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 |
|---|---|---|---|
| DRE | Dilator, Vessel, For Percutaneous Catheterization | FDA class 2 | Cardiovascular |
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