Disposable Surgical Mask

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

TIGER FLAT SURGICAL MASK

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

I_OPEN 0.4T

FDA 510(k)

FDA Class 2 ·Radiology

I OPEN 0.5T

FDA 510(k)

FDA Class 2 ·Radiology

DIGITAL PACIFIER THERMOMETER (MODEL NO.: TM-03)

FDA 510(k)

FDA Class 2 ·General Hospital

Ultraviolet Phototherapy Device

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Arm Type Automatic Blood Pressure Monitor BP310A, BP313A, BP351A, BP362A, BP366A, BP369A, BP380A, BP389A, BP-JC312

FDA 510(k)

FDA Class 2 ·Cardiovascular

Medical Endoscope Image Processing System

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

IPL Hair Removal, Model(s): SB01, SB01A, SB01B, SB01C, SN02, SN03

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Bronchoscope System, The Single-use Bronchoscope (Single-use Bronchoscope: SP-Y-ZQGJ2.8, SP-Y-ZQGJ3.8, SP-Y-ZQGJ4.2, SP-Y-ZQGJ4.8, SP-Y-ZQGJ5.2, SP-Y-ZQGJ5.8; Electronic Endoscope Imaging Processor: SP-TXCLQ12.1)

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

Infrared Thermometer

FDA 510(k)

FDA Class 2 ·General Hospital

EASY-TEST AMYLASE (AMYL), ITEM NUMBER 19019

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

TECHNICON RA-1000 SYS, ANALYTES III

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

Antisera, Hai (Including Hai Control), Rubella

FDA classification

FDA Class 2 ·Antisera, Hai (Including Hai Control), Rubella

Analyzer, Medical Image

FDA Pre-Market Approval

FDA Class 2 ·IMAGECHECKER M1000

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BRANTIGEN I/F CAGE(R) USED WITH VSP(R) SPINE PLATES AND PEDICLE SCREWS

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·INTER FIX RP THREADED FUSION DEVICE-REDUCED PROFILE

Igm (Mu Chain Specific), Antigen, Antiserum, Control

FDA classification

FDA Class 2 ·Igm (Mu Chain Specific), Antigen, Antiserum, Control

Airway, Esophageal (Obturator)

FDA classification

FDA Class 2 ·Airway, Esophageal (Obturator)

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·VISTA LORDOTIC INTERBODY FUSION CAGE