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Louisville Laboratories, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K980123CARTER-THOMASON NEEDLE-POINT SUTURE PASSER INSTRUMENT SETMarch 9, 1998
K971796LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORSAugust 12, 1997
K971791VAGINAL SUTURING KIT FOR LAPAROTOMY BLADDER NECK SUSPENSIONJuly 30, 1997
K971802VAGINAL SUTURING KIT FOR BLADDER NECK SUSPENSIONJuly 30, 1997
K971801LAPAROTOMY BLADDER NECK SUSPENSION KITJuly 22, 1997
K971797LAPAROSCOPIC BLADDER NECK SUSPENSION KITJuly 22, 1997
K963076LAPAROSCOPIC BONE ANCHORED URETHROPEXY INSTRUMENT TRAYApril 4, 1997
K960882CONTROL SYRINGEJuly 8, 1996
K955535LOUISVILLE LABS OXYGEN HEAD TENTJuly 1, 1996
K946282UNIVERSAL URETHRAL CATHETERMarch 31, 1995
K932979EXTERNAL STABILITY PADNovember 2, 1993
K894757T-SCOPE, TELEMETRIC PRECORDIAL STETHOSCOPESeptember 18, 1989