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Te ME NA S.A.R.L.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K990323TE ME NA POLYSTIM NERVE STIMILATORSeptember 28, 2001
K002405SPINAL EPIDURAL NEEDLESJune 1, 2001
K991259TE ME NA EPIDURAL CATHETERFebruary 21, 2001
K990100POLYMEDIC UPA NERVE STIMULATION NEEDLE; POLYMEDIC UPC NERVE STIMULATION NEEDLEAugust 2, 2000
K990020TE ME NA LOSS OF RESISTANCE SYRINGE, 10CCJune 24, 1999