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Keta Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K861027
KETA HAND-HELD TONOMETER
May 6, 1986
K861028
SUPERLITE PENLIGHT
April 4, 1986
K844570
QUANTUM 412
December 5, 1984