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The Sanborn Co.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K901553SURG-K SURGICAL KERATOMETERJuly 20, 1990
K901523VKG 1000, VIDEO KERATOGRAPHJune 27, 1990