Ankle Fusion Cage

FDA classification

FDA Class 2 ·Ankle Fusion Cage

Antisera, Hai (Including Hai Control), Rubella

FDA classification

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

Pipette, Sahli

FDA classification

FDA Class 1 ·Pipette, Sahli

Sars-Cov-2 Serology Test

FDA classification

FDA Class 2 ·Sars-Cov-2 Serology Test

Rongeur, Lachrymal Sac

FDA classification

FDA Class 1 ·Rongeur, Lachrymal Sac

Antiserum, Hai, Rubeola

FDA classification

FDA Class 1 ·Antiserum, Hai, Rubeola

Antiserum, Hai, Mumps Virus

FDA classification

FDA Class 1 ·Antiserum, Hai, Mumps Virus

Over-The-Counter Molecular Test To Detect Sars-Cov-2 From Clinical Specimens

FDA classification

FDA Class 2 ·Over-The-Counter Molecular Test To Detect Sars-Cov-2 From Clinical Specimens

Circuit, Breathing (W Connector, Adaptor, Y Piece)

FDA classification

FDA Class 1 ·Circuit, Breathing (W Connector, Adaptor, Y Piece)

Complement C1r, Antigen, Antiserum, Control

FDA classification

FDA Class 2 ·Complement C1r, Antigen, Antiserum, Control

Antisera, Hai, Reovirus 1-3

FDA classification

FDA Class 1 ·Antisera, Hai, Reovirus 1-3

Antisera, Hai, Adenovirus 1-33

FDA classification

FDA Class 1 ·Antisera, Hai, Adenovirus 1-33

Non-Sars Coronavirus Multiplex Nucleic Acid Assay

FDA classification

FDA Class 2 ·Non-Sars Coronavirus Multiplex Nucleic Acid Assay

Ngs Whole Genome Sequencing For Sars-Cov-2 Genetic Analysis

FDA classification

FDA Not Classified ·Ngs Whole Genome Sequencing For Sars-Cov-2 Genetic Analysis

Antisera, Hai, Parainfluenza Virus 1-4

FDA classification

FDA Class 1 ·Antisera, Hai, Parainfluenza Virus 1-4

Sensor, Pressure, Aneurysm, Implantable

FDA classification

FDA Class 2 ·Sensor, Pressure, Aneurysm, Implantable

Peripheral Blood Processing Device For Osteoarthritis

FDA classification

FDA Not Classified ·Peripheral Blood Processing Device For Osteoarthritis

Over-The-Counter Covid-19 Antigen Test

FDA classification

FDA Class 2 ·Over-The-Counter Covid-19 Antigen Test

Covid-19 Test Home Collection Kit Devices

FDA classification

FDA Not Classified ·Covid-19 Test Home Collection Kit Devices

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