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

SENSUS

K Number: K121184 · Decision Aug 2, 2012
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
605
Applicant Total
18
Review Days
106

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Basic Information

Device Name
SENSUS
K Number
K121184
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neurometrix, Inc.
Date Received
April 18, 2012
Decision Date
August 2, 2012
Product Code
GZJ
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
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief

Similar 510(k) Clearances

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

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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
K091155 ASCEND
K083322 NEUROMETRIX BIOAMPLIFIER
K083818 UNIVERSAL ELECTRODES
K081871 UNIVERSAL ELECTRODES
Search all 18 clearances from Neurometrix, Inc. →