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Telos Medical Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K920375DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCEROctober 27, 1992
K920044DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KITApril 3, 1992
K914387TRANSCERVICAL INTRAUTERINE KITDecember 30, 1991
K905018LAB-SITE SAFETY NEEDLEJanuary 16, 1991
K905017LAB-SITEJanuary 15, 1991
K882224ULTRANS DISPOSABLE INTRAUTERINEOctober 12, 1989
K883832CATHETER, INTRAUTERINE AND INTRODUCERDecember 13, 1988