Stimulation System (PA series, PR series, S series and Q series)— 510(k) K232786
Substantially EquivalentEdan Instruments, Inc.
FDA 510(k) clearance K232786 for Stimulation System (PA series, PR series, S series and Q series), Substantially Equivalent on 2024-05-16. Applicant: Edan Instruments, Inc.. Device class: 2.
Clearance details
- Applicant
- Edan Instruments, Inc.
- 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
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