Set, Dialysis, Single Needle With Uni-Directional Pump, Reprocessed

FDA classification

FDA Class 2 ·Set, Dialysis, Single Needle With Uni-Directional Pump, Reprocessed

Radioimmunoassay, Digoxin (3-H), Rabbit Antibody, Coated Tubes Sep.

FDA classification

FDA Class 2 ·Radioimmunoassay, Digoxin (3-H), Rabbit Antibody, Coated Tubes Sep.

Radioimmunoassay, Digitoxin (125-I), Rabbit Antibody, Solid Phase Sep.

FDA classification

FDA Class 2 ·Radioimmunoassay, Digitoxin (125-I), Rabbit Antibody, Solid Phase Sep.

Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.

FDA classification

FDA Class 2 ·Radioimmunoassay, Morphine (125-I), Goat Antibody Ammonium Sulfate Sep.

Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

FDA classification

FDA Class 2 ·Set, Tubing, Blood, With And Without Anti-Regurgitation Valve

Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.

FDA classification

FDA Class 2 ·Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Solid Phase Sep.

Pediatric/Child Facemask

FDA classification

FDA Class 2 ·Pediatric/Child Facemask

Simple Point-Of-Care Device To Directly Detect Sars-Cov-2 Viral Targets From Clinical Specimens In Near-Patient Settings

FDA classification

FDA Class 2 ·Simple Point-Of-Care Device To Directly Detect Sars-Cov-2 Viral Targets From Clinical Specimens In Near-Patient Settings

Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets From Clinical Specimens In Near-Patient Settings

FDA classification

FDA Class 2 ·Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets From Clinical Specimens In Near-Patient Settings

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·PRIME{TM} MODEL 6520, 6525, 6530 AND 6535

Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users

FDA classification

FDA Class 2 ·Test For Detection Of Microorganism(S) Causing Sexually Transmitted Infections Performed By Lay Users

Radioimmunoassay, Digoxin (125-I), Goat Antibody, Anion Exchange, Resin Sep.

FDA classification

FDA Class 2 ·Radioimmunoassay, Digoxin (125-I), Goat Antibody, Anion Exchange, Resin Sep.

Non-Variola Orthopoxvirus Real-Time Pcr Primer And Probe Set

FDA classification

FDA Class 2 ·Non-Variola Orthopoxvirus Real-Time Pcr Primer And Probe Set

Stationary Infrared Thermometer

FDA classification

FDA Class 2 ·Stationary Infrared Thermometer

Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay

FDA classification

FDA Class 2 ·Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay

Test For Detection Of Antibodies Associated With Syphilis Performed By Lay Users

FDA classification

FDA Class 2 ·Test For Detection Of Antibodies Associated With Syphilis Performed By Lay Users