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

GYMFORM ABS-A-ROUND

K Number: K130074 · Decision Aug 15, 2013
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
161
Applicant Total
4
Review Days
213

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
GYMFORM ABS-A-ROUND
K Number
K130074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Well Brain International , Ltd.
Date Received
January 14, 2013
Decision Date
August 15, 2013
Product Code
NGX
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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

Similar 510(k) Clearances

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

View all

Other Clearances by Well Brain International , Ltd.

K Number Device Name
K202653 Gymform Total ABS
K142055 GYMFORM ABS & CORE
K111781 GYMFORM DUAL FLEX BELT MODEL WB-162