FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

Tech Dots - Adhesive and conductive gel

K Number: K190050 · Decision Jul 19, 2019
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
68
Applicant Total
9
Review Days
190

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
Tech Dots - Adhesive and conductive gel
K Number
K190050
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1275
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spes Medica Srl
Date Received
January 10, 2019
Decision Date
July 19, 2019
Product Code
GYB
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
GYB Media, Electroconductive

Similar 510(k) Clearances

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

View all

Other Clearances by Spes Medica Srl

K Number Device Name
K211954 Subdural Electrode, Strip/Intraoperative Strip, Grid/Intraoperative Grid, Multi-Strip and Split Grid, Intraoperative Mapping Grid
K212326 AC Cream - Conductive paste
K192606 SAC2 - Electrode Cream
K192603 Spes Medica Subdermal Needle Electrodes
K133348 STIM PROBE
K120494 DISPOSABLE ADHESIVE SURFACE ELECTRODE
K093373 LARYNGEAL SURFACE ELECTRODE
K091410 DISPOSABLE EMG NEEDLE ELECTRODES, MYOLINE, MYOLINE 2, MYOBOT,