FDA 510(k)
Unknown
🇺🇸 United States
HEMO-KART
K Number: K841179
·
Decision Mar 20, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
3
Review Days
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Basic Information
- Device Name
- HEMO-KART
- K Number
- K841179
- Clearance Type
- Traditional
- Decision
- Unknown
- Applicant
- Micro Encapsulation Tech.
- Date Received
- March 20, 1984
- Decision Date
- March 20, 1984
- Advisory Committee
- Unknown
- Review Advisory Committee
- GU
- Third Party
- N