TIBIAL PLATEU

FDA 510(k)

FDA Class 2 ·Orthopedic

ICLH TIBIAL PLATEAU

FDA 510(k)

FDA Class 2 ·Orthopedic

FREEMAN-SAMUELSON MARK II PRESS-FIT TOTAL KNEE REP

FDA 510(k)

FDA Class 2 ·Orthopedic

MARK I TOTAL KNEE SYS. ARTHROPLASTY

FDA 510(k)

FDA Class 2 ·Orthopedic

TRICON M TOTAL KNEE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

QUADROX-ID ADULT DIFFUSION MEMBRANE OXYGENATOR WITH SOFTLINE COATING, MODEL: BE-HMOD 70000-USA, BEQ-HMOD 70000-USA, HMOD

FDA 510(k)

FDA Class 2 ·Cardiovascular

VENOUS BUBBLE TRAP, MODEL VBT 160; VENOUS BUBBLE TRAP WITH BIOLINE COATING, MODEL BE-VBT 160, BEQ-VBT 160

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·USCI APOLLO RELY SP OVER-THE-WIRE BALLOON DILATATION CATHETER WITH HYDRO/PEL COATING AND MINIQUET DEVICE

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·USCI GRUNTZIG DILACA CORONARY ARTERY BALLOON DILATATION CATHETER & USCI XPRT WITH PRO/PEL COATING BALLOON DILATATION

DIGI-PRO TENS MODEL WL-2203 AND WL-2205

FDA 510(k)

FDA Class 2 ·Neurology

TEMP SCAN

FDA 510(k)

FDA Class 2 ·General Hospital

IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND

FDA 510(k)

FDA Class 2 ·Neurology

THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302)

FDA 510(k)

FDA Class 2 ·Neurology

DIGI-PRO TENS, MODEL WL-2204 AND WL-2205

FDA 510(k)

FDA Class 2 ·Physical Medicine

DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205B

FDA 510(k)

FDA Class 2 ·Neurology

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·USCI(R)PROCROSS(TM) OVER THE WIRE BALLON DILATATION CATHETERT WITH RELY TM BALLOON MATERIAL AND HYDRO/PEL

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·NEPTUNE X-ACT OVER-THE-WIRE BALLOON DILATATION ACATHETER WITH HYDRO/PEL COATING AND ANTI BACK BLEED DEVICE

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·USCI(R) PROCROSS(TM) OVER-THE-WIRE BALLOON DILATION WITH RELY(TM) BALLOON MATERIAL AND HYDRO/PEL(R) COATING

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·USCI GRUNTZIG DILICA CORONARY ARTERY BALLOON DILATATION CATHETER & USCI PROCROSS ELITE OVER THE WIRE W/PRO/PEL COATING

BILIRUBIN ASSAY KIT (DIRECT), CATA. NUMBER 202-02

FDA 510(k)

FDA Class 2 ·Clinical Chemistry