FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VYGON SPLIT CANNULA INTRODUCER
K Number: K010913
·
Decision Sep 28, 2001
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
48
Review Days
185
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Basic Information
- Device Name
- VYGON SPLIT CANNULA INTRODUCER
- K Number
- K010913
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Vygon Corp.
- Date Received
- March 27, 2001
- Decision Date
- September 28, 2001
- Product Code
- DYB
- 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 |
|---|---|---|---|
| DYB | Introducer, Catheter | FDA class 2 | Cardiovascular |
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