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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