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

PALS NEONATAL PEDIATRIC ECG ELECTRODE, MODELS PN100, PN200

K Number: K000206 · Decision Apr 13, 2000
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
11
Review Days
83

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Basic Information

Device Name
PALS NEONATAL PEDIATRIC ECG ELECTRODE, MODELS PN100, PN200
K Number
K000206
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Axelgaard Mfg. Co., Ltd.
Date Received
January 21, 2000
Decision Date
April 13, 2000
Product Code
DRX
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DRX Electrode, Electrocardiograph

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Other Clearances by Axelgaard Mfg. Co., Ltd.

K Number Device Name
K132422 PALS PLATINUM NEUROSTIMULATION ELECTRODES
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K080580 COMFORT IONTOPHORESIS ELECTRODES/ BUFFERED IONTOPHORESIS ELECTRODE TREATMENT, MODEL SMALL DDS275, MEDIUM DDM325, LARGE D
K013532 ULTRASTIM KIT
K000947 ULTRASTIM ELECTRODE, MODEL US4040
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. →