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

REUSABLE DUAL DISC BAR ELECTRODES, VARIOUS MODELS

K Number: K921504 · Decision Sep 11, 1992
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
26
Applicant Total
21
Review Days
164

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Basic Information

Device Name
REUSABLE DUAL DISC BAR ELECTRODES, VARIOUS MODELS
K Number
K921504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1550
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Chalgren Enterprises, Inc.
Date Received
March 31, 1992
Decision Date
September 11, 1992
Product Code
JXE
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
JXE Device, Nerve Conduction Velocity Measurement

Similar 510(k) Clearances

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

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Other Clearances by Chalgren Enterprises, Inc.

K Number Device Name
K982950 FINE WIRE ELECTRODE MMODEL NUMBERS 221-14-730, 221-24-730, 221-14-550, 221-24-550
K960591 RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP
K955335 DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE
K953356 EMG RECORDING RING ELECTRODE
K953354 EMG DISC RECORDING ELECTRODE
K953361 EMG DISC RECORDING ELECTRODE
K952690 EMG DISC RECORDING ELECTRODE WITH PIN
K952908 EMG DISC RECORDING ELECTRODE WITH PIN
K953886 RE-USABLE MONOPOLAR NEEDLE
K953887 RE-USABLE CONCENTRIC NEEDLE
Search all 21 clearances from Chalgren Enterprises, Inc. →