Omni Intl., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K984066OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIMJanuary 13, 1999
K984064OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREEJanuary 8, 1999
K853255OMNIMED I.V. SOLUTION ADMIN. SETAugust 23, 1985
K851938OMNIMED SURGICAL GOWNJune 28, 1985
K851654OMNIMED CLAMPMay 31, 1985
K851734OMNIMED SUPERIOR TRANSDUCER PROTECTORMay 23, 1985
K850706F-SERIES IMPLANTApril 10, 1985
K850112OMNIMED IV SOLUTION ADMINISTRATION SETFebruary 22, 1985
K850066OMNIMED NASAL OXYGEN CANNULAJanuary 24, 1985
K831147OMNIPROBE ELECTRICAL NERVE STIMULATORJuly 18, 1983
K821523OMNI TENSJune 16, 1982
K813604OMNI STIM IIMarch 8, 1982