FDA 510(k) FDA unclassified Substantially Equivalent 🇨🇳 China

JIAJIAN ELECTRO-ACUPUNCTURE STIMULATORS

K Number: K122812 · Decision Apr 11, 2013
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
22
Applicant Total
12
Review Days
210

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Basic Information

Device Name
JIAJIAN ELECTRO-ACUPUNCTURE STIMULATORS
K Number
K122812
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wuxi Jiajian Medical Instrument Co., Ltd.
Date Received
September 13, 2012
Decision Date
April 11, 2013
Product Code
BWK
Advisory Committee
Unknown
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
BWK Stimulator, Electro-Acupuncture

Similar 510(k) Clearances

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Other Clearances by Wuxi Jiajian Medical Instrument Co., Ltd.

K Number Device Name
K244030 Needle Stimulator (CMNS6-1 PLUS, CMNS6-3)
K231425 Transcutaneous Electrical Nerve Stimulator (TENS WMPS2-1)
K222879 Transcutaneous Electrical Nerve Stimulator (model: TENS WMPS6-1)
K202861 Needle Stimulator
K202893 Transcutaneous Electrical Nerve Stimulator
K192568 Jiajian Self-Adhesive Electrode
K123958 JIAJIAN POINTOSELECT DIGITAL
K130768 JIAJIAN CMN STIMULATOR
K112288 JIAJIAN TENS
K090199 JIAJIAN ACUPUNCTURE NEEDLE
Search all 12 clearances from Wuxi Jiajian Medical Instrument Co., Ltd. →