LifePak 500 AED

FDA registration

EMS SURPLUS CANADA·1 product·🇨🇦 Canada

MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA 510(k)

FDA Class 3 ·Cardiovascular

Automated External Defibrillators (Non-Wearable)

FDA classification

FDA Class 3 ·Automated External Defibrillators (Non-Wearable)

Acuvance

FDA registration

ICU Medical, Inc.·1 product·🇺🇸 United States

Triceram

FDA registration

Dentaurum GmbH & Co. KG·1 product·🇩🇪 Germany

Catheter, Intravascular, Therapeutic, Short-term Less than 30 days - DeRoyal

FDA registration

DEROYAL INDUSTRIES, INC.·1 product·🇺🇸 United States

STERILIZATION SERVICES OF VIRGINIA

FDA registration

STERILIZATION SERVICES OF VIRGINIA·1 product·🇺🇸 United States

Catheter, Intravascular, Therapeutic, Short-term Less than 30 days - DeRoyal

FDA registration

DeRoyal Industries, Inc.·1 product·🇺🇸 United States

Acuvance

FDA registration

ICU Medical, Inc.·1 product·🇺🇸 United States

Catheter, Intravascular, Therapeutic, Short-term Less than 30 days - DeRoyal

FDA registration

DEROYAL INDUSTRIES, INC.·1 product·🇺🇸 United States

Catheter, Intravascular, Therapeutic, Short-term Less than 30 days - DeRoyal

FDA registration

DEROYAL INDUSTRIES, INC.·1 product·🇺🇸 United States

ACCUTNI QC ON THE ACCESS IMMUNOASSAY SYSTEM #33349

FDA 510(k)

FDA Class 1 ·Clinical Chemistry

TRICERAM

FDA 510(k)

FDA Class 2 ·Dental

Single (Specified) Analyte Controls (Assayed And Unassayed)

FDA classification

FDA Class 1 ·Single (Specified) Analyte Controls (Assayed And Unassayed)

Powder, Porcelain

FDA classification

FDA Class 2 ·Powder, Porcelain