FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DISPOSABLE STOPCOCKS
K Number: K842173
·
Decision Sep 5, 1984
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
88
Applicant Total
16
Review Days
113
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Basic Information
- Device Name
- DISPOSABLE STOPCOCKS
- K Number
- K842173
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Procedure Products, Inc.
- Date Received
- May 15, 1984
- Decision Date
- September 5, 1984
- 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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FDA 510(k)
FDA Class 2
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