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

EEG MIS MONITOR MODEL # A-2000; BIS ENGINE

K Number: K011534 · Decision Jun 15, 2001
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
37
Applicant Total
25
Review Days
28

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Basic Information

Device Name
EEG MIS MONITOR MODEL # A-2000; BIS ENGINE
K Number
K011534
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aspect Medical Systems, Inc.
Date Received
May 18, 2001
Decision Date
June 15, 2001
Product Code
OLW
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
OLW Index-Generating Electroencephalograph Software

Similar 510(k) Clearances

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

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Other Clearances by Aspect Medical Systems, Inc.

K Number Device Name
K093183 BIS QUATRO SENSOR
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
Search all 25 clearances from Aspect Medical Systems, Inc. →