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

Electric Wheelchair (Robooter E40), Model name: BBR-E40-01

K Number: K231868 · Decision Oct 31, 2023
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
4
Review Days
127

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Basic Information

Device Name
Electric Wheelchair (Robooter E40), Model name: BBR-E40-01
K Number
K231868
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Shanghai Bangbang Robotics Co., Ltd.
Date Received
June 26, 2023
Decision Date
October 31, 2023
Product Code
ITI
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
ITI Wheelchair, Powered

Similar 510(k) Clearances

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

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Other Clearances by Shanghai Bangbang Robotics Co., Ltd.

K Number Device Name
K253276 Electric Wheelchair (Robooter E80) (BBR-E80-01); Electric Wheelchair (Robooter E80) (BBR-E80-02)
K240339 Electric Wheelchair (Robooter E60) (BBR-E60-01); Electric Wheelchair (Robooter E60) (BBR-E60-02); Electric Wheelchair (Robooter E60) (BBR-E60-03); Electric Wheelchair (Robooter E60) (BBR-E60-04); Electric Wheelchair (Robooter E60) (BBR-E60-05); Electric Wheelchair (Robooter E60) (BBR-E60-06); Electric Wheelchair (Robooter E60) (BBR-E60-07); Electric Wheelchair (Robooter E60) (BBR-E60-08)
K223393 Electric Wheelchair