The Sanborn Co.

FDA Regulatory Profile

The Sanborn Co. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 20, 1990.

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