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

MODIFICATION TO:NESS L300

K Number: K080219 · Decision Feb 28, 2008
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
60
Applicant Total
7
Review Days
30

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
MODIFICATION TO:NESS L300
K Number
K080219
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5810
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ness-Neuromuscular Electrical Stimulation Systems
Date Received
January 29, 2008
Decision Date
February 28, 2008
Product Code
GZI
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
GZI Stimulator, Neuromuscular, External Functional

Similar 510(k) Clearances

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

View all

Other Clearances by Ness-Neuromuscular Electrical Stimulation Systems

K Number Device Name
K111767 NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT
K053468 NESS L300
K031900 HANDMASTER
K024279 NESS CHILDREN SYSTEM
K022776 NESS SYSTEM
K012823 MODIFICATION TO HANDMASTER