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

NESS SYSTEM

K Number: K022776 · Decision Sep 11, 2002
Classifications
1
FEI Numbers
170
Registration Numbers
170
Same Product Code
547
Applicant Total
7
Review Days
21

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Basic Information

Device Name
NESS SYSTEM
K Number
K022776
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ness-Neuromuscular Electrical Stimulation Systems
Date Received
August 21, 2002
Decision Date
September 11, 2002
Product Code
IPF
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IPF Stimulator, Muscle, Powered

Similar 510(k) Clearances

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

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Other Clearances by Ness-Neuromuscular Electrical Stimulation Systems

K Number Device Name
K111767 NESS H200 WIRELESS HAND REHABILITATION SYSTEM USER KIT AND CLINICAN KIT
K080219 MODIFICATION TO:NESS L300
K053468 NESS L300
K031900 HANDMASTER
K024279 NESS CHILDREN SYSTEM
K012823 MODIFICATION TO HANDMASTER