FDA 510(k) Substantially Equivalent 🇺🇸 United States

STANDEX SYSTEM

K Number: K837178 · Decision Mar 22, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
94
Review Days
34

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Basic Information

Device Name
STANDEX SYSTEM
K Number
K837178
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Elscint, Inc.
Date Received
February 16, 1983
Decision Date
March 22, 1983
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

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