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

Cervello STIM

K Number: K151354 · Decision Jan 27, 2016
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
31
Applicant Total
1
Review Days
252

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
Cervello STIM
K Number
K151354
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1310
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Blackrock Neuromed
Date Received
May 20, 2015
Decision Date
January 27, 2016
Product Code
GYC
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
GYC Electrode, Cortical

Similar 510(k) Clearances

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

View all