FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

EASYSTIM TN28_OTC

K Number: K140168 · Decision Aug 28, 2014
Classifications
1
FEI Numbers
160
Registration Numbers
160
Same Product Code
227
Applicant Total
3
Review Days
217

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
EASYSTIM TN28_OTC
K Number
K140168
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5890
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Easymed Instruments Co., Ltd.
Date Received
January 23, 2014
Decision Date
August 28, 2014
Product Code
NUH
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
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter

Similar 510(k) Clearances

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

View all

Other Clearances by Easymed Instruments Co., Ltd.

K Number Device Name
K241899 Pelvic Floor Stimulator (Intrelief PFE)
K211263 Intrelief