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

DISPOSABLE THERAPY ELECTRODE

K Number: K924473 · Decision May 19, 1993
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
436
Applicant Total
12
Review Days
261

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DISPOSABLE THERAPY ELECTRODE
K Number
K924473
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1320
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Zimmer Elektromedizin GmbH
Date Received
August 31, 1992
Decision Date
May 19, 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

Similar 510(k) Clearances

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

View all

Other Clearances by Zimmer Elektromedizin GmbH

K Number Device Name
K080735 CRYOMINI
K060395 CRYO, MODEL V6.0
K040727 CRYO 5
K960969 GALVA 5-T
K952536 SONO 5
K954411 GALVA-5-M
K860758 VACO SUCTION ELECTRODE UNIT
K850006 TENS
K852166 THERMO SHORTWAVE DIATHERMY
K850453 SINUS AC-POWERED MUSCLE STIMULATOR
Search all 12 clearances from Zimmer Elektromedizin GmbH →