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Metrix Teknika, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K781803
FILTER, EYRPUR DISPOSABLE LEUKOCITE
January 17, 1979
K781802
WASHER SYSTEM, MICROELISA
December 20, 1978
K781348
FOCISCAN ECHOVISOR SYSTEM
October 3, 1978
K780035
MINIVISOR
March 6, 1978