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Midwest Eye Laboratories, Inc.

FDA Regulatory Profile

Midwest Eye Laboratories, Inc. appears in FDA public data with 0 recalls, 2 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 30, 1991.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K904962EYE ARTIFICIAL CUSTOMAugust 30, 1991
K904961ARTIFICIAL SCLERAL SHELLAugust 30, 1991

FDA data resources