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Seiko Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K900732
SPECTACLE FRAME
June 20, 1990
K884360
SEIKO P-6 PROGRESSIVE SPECTACLE LENSES
November 15, 1988