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)— 510(k) K212948
Substantially EquivalentGuangzhou Xinbo Electronic Co., Ltd.
FDA 510(k) clearance K212948 for 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), Substantially Equivalent on 2021-11-01. Applicant: Guangzhou Xinbo Electronic Co., Ltd..
Clearance details
- Applicant
- Guangzhou Xinbo Electronic Co., Ltd.
- Product code
- Code NGX
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Guangzhou, CN
Data sourced from openFDA. This site is unofficial and independent of the FDA.