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

TOMEY PE-400 PORTABLE ERG & VEP WITH OPTIONAL PS-4

K Number: K932571 · Decision Aug 31, 1995
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
48
Applicant Total
9
Review Days
826

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
TOMEY PE-400 PORTABLE ERG & VEP WITH OPTIONAL PS-4
K Number
K932571
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tomey Corporation USA
Date Received
May 27, 1993
Decision Date
August 31, 1995
Product Code
GWE
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GWE Stimulator, Photic, Evoked Response

Similar 510(k) Clearances

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

View all

Other Clearances by Tomey Corporation USA

K Number Device Name
K971953 CONFOSCAN
K971685 IMAGESCAPE DIGITAL RETINAL IMAGE SYSTEM
K961805 TOMEY DTL ELECTRODE
K945959 VIDEO VISION ANALYZER (VIVA), VRB 100
K944910 TOMEY EM-1000 SPECULAR MICROSCOPE
K924760 TOMEY PROTON TONOMETER
K921815 TOMEY PE-300 PORTABLE ERG
K912112 PF-400,GF-300,IF-200,PG400,PG400C,AND ED-480