Biofeedback Nerve and Muscle Stimulator— 510(k) K202648
Substantially EquivalentShenzhen Konmed Technology Co., Ltd.
FDA 510(k) clearance K202648 for Biofeedback Nerve and Muscle Stimulator, Substantially Equivalent on 2020-12-08. Applicant: Shenzhen Konmed Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Konmed Technology Co., Ltd.
- Product code
- Code IPF
- Device class
- Class 2
- Regulation
- 21 CFR 890.5850
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
Recent devices under product code IPF
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- K220161 — Biofeedback Nerve and Muscle Stimulator
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Data sourced from openFDA. This site is unofficial and independent of the FDA.