FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PORTABLE MEDICAL ULTRASOUND SCANNER

K Number: K800434 · Decision Apr 10, 1980
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
14
Review Days
43

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PORTABLE MEDICAL ULTRASOUND SCANNER
K Number
K800434
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Bion Ent., Ltd.
Date Received
February 27, 1980
Decision Date
April 10, 1980
Product Code
IYO
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IYO), ordered by most recent decision date.

View all

Other Clearances by Bion Ent., Ltd.

K Number Device Name
K926066 BION MUMPS-G ANTIBODY TEST SYSTEM
K901054 BION BORRELIA BURGDORFERI ANTIGEN SUBSTRATE SLIDE
K894622 VARICELLA ZOSTER VIRUS
K894624 MUMPS VIRUS
K894623 RESPIRATORY SYNCYTIAL VIRUS
K894626 EPSTEIN-BARR VIRUS-NUCLEAR ANTIGEN
K891785 BION EBV-G (VCA) TEST SYSTEM
K894625 CHLAMYDIA (LGV-1)
K893240 BION EBV-M (VCA) TEST SYSTEM
K890616 BION DIRECT IDENTIFICATION CONTROL SLIDE
Search all 14 clearances from Bion Ent., Ltd. →