FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
KHM 2000 DRIP WATCHER
K Number: K844556
·
Decision Jan 14, 1985
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
38
Applicant Total
4
Review Days
54
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Basic Information
- Device Name
- KHM 2000 DRIP WATCHER
- K Number
- K844556
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.2420
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- The Timeter Group
- Date Received
- November 21, 1984
- Decision Date
- January 14, 1985
- Product Code
- FLN
- 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 |
|---|---|---|---|
| FLN | Monitor, Electric For Gravity Flow Infusion Systems | FDA class 2 | General Hospital |
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