Last synced on 9 May 2025 at 11:05 pm

Konmed Incontinence Stimulation Electrode (Vaginal Probe: KM-503, KM-504, KM-505, KM-506, KM-507, KM-5013; Rectal Probe: KM-502, KM-5018)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233576
510(k) Type
Traditional
Applicant
Shenzhen Konmed Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/23/2024
Days to Decision
108 days
Submission Type
Statement

Konmed Incontinence Stimulation Electrode (Vaginal Probe: KM-503, KM-504, KM-505, KM-506, KM-507, KM-5013; Rectal Probe: KM-502, KM-5018)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233576
510(k) Type
Traditional
Applicant
Shenzhen Konmed Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
2/23/2024
Days to Decision
108 days
Submission Type
Statement