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

QMED SELF ADHERING ELECTRODE

K Number: K862377 · Decision Sep 26, 1986
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
11
Review Days
94

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Basic Information

Device Name
QMED SELF ADHERING ELECTRODE
K Number
K862377
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Qmed, Inc.
Date Received
June 24, 1986
Decision Date
September 26, 1986
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 Qmed, Inc.

K Number Device Name
K972991 MONITOR ONE NDX
K932109 PROFILOMAT
K921476 INTERP-1000
K897121 QEKG ELECTROCARDIOGRAPH
K873591 A.R.M. (ASPEN RETURN MONITOR)
K863091 BICORD BY QMED
K861437 QMED SYSTEM 2150
K843559 KLEENIT BY QMED
K841172 MONITOR ONE
K840465 Q-MED ELECTRODE
Search all 11 clearances from Qmed, Inc. →