Multicept, Aps.

FDA Regulatory Profile

Multicept, Aps. 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 April 11, 1996.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K955589FERTICARE PERSONAL THERAPEUTIC VIBRATORApril 11, 1996
K851646VIBRECTORAugust 21, 1985