FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MANIFOLD, DISPOSABLE 3 VALVE
K Number: K790010
·
Decision Feb 1, 1979
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
88
Applicant Total
315
Review Days
30
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Basic Information
- Device Name
- MANIFOLD, DISPOSABLE 3 VALVE
- K Number
- K790010
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Cordis Corp.
- Date Received
- January 2, 1979
- Decision Date
- February 1, 1979
- Product Code
- FMG
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FMG | Stopcock, I.V. Set | FDA class 2 | General Hospital |
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