Last synced on 25 April 2025 at 11:05 pm

Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231789
510(k) Type
Traditional
Applicant
Guangzhou Xinbo Electronic Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/11/2024
Days to Decision
265 days
Submission Type
Statement

Pain Therapy Device (Model: P.T.S-VI, P.T.S-VII)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231789
510(k) Type
Traditional
Applicant
Guangzhou Xinbo Electronic Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
3/11/2024
Days to Decision
265 days
Submission Type
Statement