Last synced on 24 May 2024 at 11:04 pm

EMS/TENS Massager Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233040
510(k) Type
Traditional
Applicant
Shenzhen IMDK Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/12/2024
Days to Decision
140 days
Submission Type
Statement

EMS/TENS Massager Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233040
510(k) Type
Traditional
Applicant
Shenzhen IMDK Medical Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/12/2024
Days to Decision
140 days
Submission Type
Statement