Last synced on 25 January 2026 at 3:41 am

8ch Flex Suite

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172222
510(k) Type
Traditional
Applicant
Shenzhen RF Tech Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/8/2017
Days to Decision
137 days
Submission Type
Summary

8ch Flex Suite

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172222
510(k) Type
Traditional
Applicant
Shenzhen RF Tech Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/8/2017
Days to Decision
137 days
Submission Type
Summary