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

DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K

K Number: K952176 · Decision Sep 25, 1995
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
14
Review Days
140

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Basic Information

Device Name
DISPOSABLE NEUROLOGY ELECTRODES NEUROLINE 7 30 01-K
K Number
K952176
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
May 8, 1995
Decision Date
September 25, 1995
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
K941568 K-10-VS, DA-05-VS, RECORDING ELECTRODES
K931426 NF-11-E DISPOSABLE REFERENCE/RECORDING ELECTRODE
K931430 CUTANEOUS 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. →