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

SKINTACT

K Number: K140500 · Decision Jul 29, 2014
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
17
Review Days
152

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Basic Information

Device Name
SKINTACT
K Number
K140500
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Leonhard Lang GmbH
Date Received
February 27, 2014
Decision Date
July 29, 2014
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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Other Clearances by Leonhard Lang GmbH

K Number Device Name
K142803 Skintact, various other tradenames
K140340 SKINTACT
K103186 SKINTACT RADIOTRANSPARENT MULTIFUNCTION ELECTRODES
K092291 SKINTACT AND VARIOUS OTHER TRADENAMES
K081371 SKINTACT PEDIATRIC MULTIFUNCTION ELECTRODES WITH DH03 GEL
K080106 SKINTACT PRE-WIRED ECG ELECTRODES WITH CONDUCTIVE ADHESIVE
K073104 SKINTACT AND VARIOUS OTHER TRADENAMES
K072233 SKINTACT MULTIFUNCTIONAL ELECTRODES WITH DH02 GEL WITH DIFFERENT CONNECTORS COMPATIBLE WITH DIFFERENT DEFIBRILLATORS
K063161 SKINTACT COOL CONTACT ELECTROSURGICAL GROUNDING PLATE WITH NH 04 GEL
K041883 SKINTACT MULTIFUNCTION ELECTRODES, MODEL DF 21
Search all 17 clearances from Leonhard Lang GmbH →