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

GALILEO EVOKED POTENTIALRE

K Number: K963662 · Decision Feb 26, 1997
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
39
Review Days
166

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
GALILEO EVOKED POTENTIALRE
K Number
K963662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biosound, Inc.
Date Received
September 13, 1996
Decision Date
February 26, 1997
Product Code
GWF
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
GWF Stimulator, Electrical, Evoked Response

Similar 510(k) Clearances

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

View all

Other Clearances by Biosound, Inc.

K Number Device Name
K971700 BIOPSY ACCESSORY FOR ULTRASOUND TRANSDUCER
K963936 ACCESSPOINT, MED E-MAIL, DICOM READER
K963262 ARTOSCAN M
K953716 INTRACAVITY TRANSDUCERS
K953530 DIAGNOSTIC ULTRASOUND TRANDUCERS P10A, P12A, PT10A, PA11-A
K953819 DIAGNOSTIC ULTRASOUND TRANDUCER
K953759 DIAGNOSTIC ULTRASOUND TRANSDUCER
K955458 ULTRASOUND PROBE BIOPSY ACCESSORIES
K953579 TEE PROBE
K953430 ULTRASOUND PROBE BIOPSY ACCESSORIES
Search all 39 clearances from Biosound, Inc. →