Hankscraft Div. of Gerber Products Co.

FDA Regulatory Profile

Hankscraft Div. of Gerber Products 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 February 15, 1985.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K844013CARE ELECTRIC BREAST PUMPFebruary 15, 1985
K790966ULTRASONIC HUMIDIFIERJune 11, 1979