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

ASCEND

K Number: K091155 · Decision Sep 3, 2009
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
62
Applicant Total
18
Review Days
135

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Basic Information

Device Name
ASCEND
K Number
K091155
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2775
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neurometrix, Inc.
Date Received
April 21, 2009
Decision Date
September 3, 2009
Product Code
BXN
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BXN Stimulator, Nerve, Battery-Powered

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Other Clearances by Neurometrix, Inc.

K Number Device Name
DEN210046 Quell-FM
K152954 Quell
K140586 ASCEND ELECTRODE
K140333 ASCEND
K130919 SENSUS
K121816 SENSUS ELECTRODE
K121184 SENSUS
K083322 NEUROMETRIX BIOAMPLIFIER
K083818 UNIVERSAL ELECTRODES
K081871 UNIVERSAL ELECTRODES
Search all 18 clearances from Neurometrix, Inc. →