KONICAMINOLTA DI-X1

FDA registration

KONICA MINOLTA, INC.·1 product·🇯🇵 Japan

KONICAMINOLTA DI-X1

FDA registration

KONICA MINOLTA, INC.·1 product·🇯🇵 Japan

KONICAMINOLTA DI-X1

FDA registration

KONICA MINOLTA TECHNOPRODUCTS CO., LTD.·1 product·🇯🇵 Japan

KONICAMINOLTA DI-X1

FDA 510(k)

FDA Class 2 ·Radiology

Isomedix Operations, Inc.

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

Sterigenics U.S., LLC

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

BrainView QEEG

FDA registration

MEDEIA INC·1 product·🇺🇸 United States

Eon Aligner

FDA registration

GC AMERICA INC.·1 product·🇺🇸 United States

BrainView QEEG

FDA registration

MEDEIA GROUP LTD·1 product·🇧🇬 Bulgaria

REPROCESSED ENDOSCOPIC ELECTRODES

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

ANGIOSCULPT PTA SCORING BALLOON CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Electrode, Electrosurgical, Active, Urological, Reprocessed

FDA classification

FDA Class 2 ·Electrode, Electrosurgical, Active, Urological, Reprocessed

Catheter, Percutaneous, Cutting/Scoring

FDA classification

FDA Class 2 ·Catheter, Percutaneous, Cutting/Scoring

System, Image Processing, Radiological

FDA classification

FDA Class 2 ·System, Image Processing, Radiological