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

CUTANEOUS ELECTRODE

K Number: K931430 · Decision Dec 21, 1993
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
14
Review Days
274

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Basic Information

Device Name
CUTANEOUS ELECTRODE
K Number
K931430
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medicotest, Inc.
Date Received
March 22, 1993
Decision Date
December 21, 1993
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

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Other Clearances by Medicotest, Inc.

K Number Device Name
K983597 NEUROLINE, DISPOSABLE MONOPOLAR NEEDLE ELECTRODES
K970639 NEUROLINE, DISPOSABLE REFERENCE AND RECORDING ELECTRODES TYPE NO: 72000-S, 72010-K
K961643 MEDICOTEST ECG ELECTRODES
K952176 DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K
K941568 K-10-VS, DA-05-VS, RECORDING ELECTRODES
K931426 NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODE
K926264 MEDICOTEST SKIN FIX
K921579 BR-50-J DISPOSABLE ECG ELECTRODE
K914672 QR-50-E DISPOSABLE RADIOTRANSLUCENT ECG ELECTRODE
K902407 NF-50-E DISPOSABLE ECG ELECTRODE
Search all 14 clearances from Medicotest, Inc. →