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Dutton-Lainson Co.

FDA Regulatory Profile

Dutton-Lainson Co. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 1, 1994.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K930624SANITAS WHIRPOOL BATHING SYSTEMJuly 1, 1994
K930625SANITAS PATIENT LIFTSeptember 13, 1993
K930626SANITAS PATIENT SCALEAugust 6, 1993

FDA data resources