Louisville Laboratories, Inc.
Louisville Laboratories, Inc. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1998.
Top product codes for Louisville Laboratories, Inc.
Recent clearances by Louisville Laboratories, Inc.
- K980123 — CARTER-THOMASON NEEDLE-POINT SUTURE PASSER INSTRUMENT SET
- K971796 — LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS
- K971791 — VAGINAL SUTURING KIT FOR LAPAROTOMY BLADDER NECK SUSPENSION
- K971802 — VAGINAL SUTURING KIT FOR BLADDER NECK SUSPENSION
- K971797 — LAPAROSCOPIC BLADDER NECK SUSPENSION KIT
- K971801 — LAPAROTOMY BLADDER NECK SUSPENSION KIT
- K963076 — LAPAROSCOPIC BONE ANCHORED URETHROPEXY INSTRUMENT TRAY
- K960882 — CONTROL SYRINGE
- K955535 — LOUISVILLE LABS OXYGEN HEAD TENT
- K946282 — UNIVERSAL URETHRAL CATHETER
- K932979 — EXTERNAL STABILITY PAD
- K894757 — T-SCOPE, TELEMETRIC PRECORDIAL STETHOSCOPE
Data sourced from openFDA. This site is unofficial and independent of the FDA.