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Low-Frequency Therapy Instrument /Model: KTR-201, KTR-202, KTR-203

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170205
510(k) Type
Traditional
Applicant
Shenzhen Kentro Medical Electronics Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/11/2017
Days to Decision
108 days
Submission Type
Summary

Low-Frequency Therapy Instrument /Model: KTR-201, KTR-202, KTR-203

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170205
510(k) Type
Traditional
Applicant
Shenzhen Kentro Medical Electronics Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/11/2017
Days to Decision
108 days
Submission Type
Summary