Last synced on 18 April 2025 at 11:05 pm

Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250033
510(k) Type
Traditional
Applicant
Guangzhou Pinzhi Medical Technology Co., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/7/2025
Days to Decision
90 days
Submission Type
Statement

Smart Pulse Relief (PZ-2622, PZ-2622T, PZ-2622E)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250033
510(k) Type
Traditional
Applicant
Guangzhou Pinzhi Medical Technology Co., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/7/2025
Days to Decision
90 days
Submission Type
Statement