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

VALUTRODE NEUROSTIMLATION ELECTRODES

K Number: K130987 · Decision Jul 17, 2013
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
11
Review Days
99

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
VALUTRODE NEUROSTIMLATION ELECTRODES
K Number
K130987
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Axelgaard Mfg. Co., Ltd.
Date Received
April 9, 2013
Decision Date
July 17, 2013
Product Code
GXY
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
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 Axelgaard Mfg. Co., Ltd.

K Number Device Name
K132422 PALS PLATINUM NEUROSTIMULATION ELECTRODES
K080580 COMFORT IONTOPHORESIS ELECTRODES/ BUFFERED IONTOPHORESIS ELECTRODE TREATMENT, MODEL SMALL DDS275, MEDIUM DDM325, LARGE D
K013532 ULTRASTIM KIT
K000947 ULTRASTIM ELECTRODE, MODEL US4040
K000206 PALS NEONATAL PEDIATRIC ECG ELECTRODE, MODELS PN100, PN200
K983741 EVERLAST NEUROSTIMULATION ELECTRODES 2X 2,MODEL # EL2020
K970426 VALUETRODE
K874469 TRANSCUTANEOUS ELECTRIC NERVE STIMULATION (TENS)
K872976 TENS PALS PLUS
K852267 ELECTRICAL NERVE STIMULATION(TENS) ELECTRODES
Search all 11 clearances from Axelgaard Mfg. Co., Ltd. →