Last synced on 20 December 2024 at 11:05 pm

Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341, KTR-2342, KTR-2401, KTR-2402, KTR-2411, KTR-2412, KTR-2491, KTR-2492, KTR-2493, KTR-2494)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242332
510(k) Type
Traditional
Applicant
Shenzhen Kentro Medical Electronics Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/5/2024
Days to Decision
90 days
Submission Type
Statement

Transcutaneous Electronic Nerve Stimulator (KTR-2301, KTR-2302, KTR-2341, KTR-2342, KTR-2401, KTR-2402, KTR-2411, KTR-2412, KTR-2491, KTR-2492, KTR-2493, KTR-2494)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K242332
510(k) Type
Traditional
Applicant
Shenzhen Kentro Medical Electronics Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/5/2024
Days to Decision
90 days
Submission Type
Statement