FDA 510(k) Substantially Equivalent 🇺🇸 United States

GLAUKON

K Number: K812015 · Decision Feb 8, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
4
Review Days
206

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Basic Information

Device Name
GLAUKON
K Number
K812015
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Sonometrics Systems, Inc.
Date Received
July 17, 1981
Decision Date
February 8, 1982
Advisory Committee
Unknown
Review Advisory Committee
OP
Third Party
N

Other Clearances by Sonometrics Systems, Inc.

K Number Device Name
K820751 GLAUKON
K802341 DIOSCAN
K781543 ORBIOGRAPH