Last synced on 25 April 2025 at 11:05 pm

Pain Therapy Device(Model: DH-P.T.S-I, DH-P.T.S-II, DH-P.T.S-IIA, DH-P.T.S-IIB, DH-CP-I)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212948
510(k) Type
Traditional
Applicant
Guangzhou Xinbo Electronic Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/1/2021
Days to Decision
46 days
Submission Type
Statement

Pain Therapy Device(Model: DH-P.T.S-I, DH-P.T.S-II, DH-P.T.S-IIA, DH-P.T.S-IIB, DH-CP-I)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212948
510(k) Type
Traditional
Applicant
Guangzhou Xinbo Electronic Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/1/2021
Days to Decision
46 days
Submission Type
Statement