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Multicept, Aps.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K955589
FERTICARE PERSONAL THERAPEUTIC VIBRATOR
April 11, 1996
K851646
VIBRECTOR
August 21, 1985