FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193
K Number: K851479
·
Decision Jun 14, 1985
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
48
Review Days
60
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Basic Information
- Device Name
- VYGON BALLOON FOR IDENTIFICATION OF EPIDURAL 193
- K Number
- K851479
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5140
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Vygon Corp.
- Date Received
- April 15, 1985
- Decision Date
- June 14, 1985
- Product Code
- CAZ
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| CAZ | Anesthesia Conduction Kit | FDA class 2 | Anesthesiology |
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