FDA 510(k)
Substantially Equivalent
🇺🇸 United States
CART, INSTRUMENT
K Number: K880536
·
Decision Feb 24, 1988
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
57
Review Days
15
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Basic Information
- Device Name
- CART, INSTRUMENT
- K Number
- K880536
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Ferguson Medical
- Date Received
- February 9, 1988
- Decision Date
- February 24, 1988
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- Third Party
- N
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