FDA 510(k) Substantially Equivalent 🇺🇸 United States

NEOSERV 824

K Number: K900729 · Decision Jun 8, 1990
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
38
Review Days
113

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Basic Information

Device Name
NEOSERV 824
K Number
K900729
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Burdick Corp.
Date Received
February 15, 1990
Decision Date
June 8, 1990
Product Code
MCJ
Advisory Committee
Unknown
Review Advisory Committee
OR
Third Party
N

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