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

THE GALILEO LINE -- PLANET 100, 200 & 300 & STAR

K Number: K923860 · Decision Feb 4, 1993
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
39
Review Days
188

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Basic Information

Device Name
THE GALILEO LINE -- PLANET 100, 200 & 300 & STAR
K Number
K923860
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Biosound, Inc.
Date Received
July 31, 1992
Decision Date
February 4, 1993
Product Code
GWQ
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
GWQ Full-Montage Standard Electroencephalograph

Similar 510(k) Clearances

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

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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
K963662 GALILEO EVOKED POTENTIALRE
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
Search all 39 clearances from Biosound, Inc. →