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

BIS QUATRO SENSOR

K Number: K093183 · Decision Oct 23, 2009
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
25
Review Days
14

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
BIS QUATRO SENSOR
K Number
K093183
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aspect Medical Systems, Inc.
Date Received
October 9, 2009
Decision Date
October 23, 2009
Product Code
GXY
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
Y

Classifications

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

Product Code Device Name
GXY Electrode, Cutaneous

Similar 510(k) Clearances

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

View all

Other Clearances by Aspect Medical Systems, Inc.

K Number Device Name
K091854 BIS CLICK SENSOR/CABLE
K072286 BIS EEG VISTA MONITOR SYSTEM AND BISX
K062613 BIS EEG MONITOR VIEW
K070069 ZIPPREP ELECTRODE
K062692 BIS BILATERAL SENSOR
K052981 BIS EEG MONITOR, MODEL BISX4
K052362 BIS EEG MONITOR, MODEL A-3000
K050313 BIS SRS (SEMI-RESUABLE SENSOR)
K041670 BIS PEDIATRIC SENSOR
K040183 BISX
Search all 25 clearances from Aspect Medical Systems, Inc. →