TENS 4100— 510(k) K792502
Substantially EquivalentStaodynamics, Inc.
FDA 510(k) clearance K792502 for TENS 4100, Substantially Equivalent on 1979-12-18. Applicant: Staodynamics, Inc.. Device class: 2.
Clearance details
- Applicant
- Staodynamics, Inc.
- Product code
- Code GZJ
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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