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Seiko Optical Products of America, Inc.

FDA Regulatory Profile

Seiko Optical Products of America, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 15, 1994.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K942513SEIKO EYEGLASS FRAMEJuly 15, 1994
K900764SUNGLASS, NON-PRESCRIPTIONJune 20, 1990
K873245AR DIACOAT SINGLE VISION LENSESOctober 5, 1987
K861684SEIKO P-2 & SEIKO P-3 (SPECTACLE LENS)June 9, 1986

FDA data resources