MUSCLESENSE ELECTROMYOGRAPHY DEVICE— 510(k) K951350
Substantially EquivalentSmith and Nephew Donjoy, Inc.
FDA 510(k) clearance K951350 for MUSCLESENSE ELECTROMYOGRAPHY DEVICE, Substantially Equivalent on 1995-06-23. Applicant: Smith and Nephew Donjoy, Inc.. Device class: 2.
Clearance details
- Applicant
- Smith and Nephew Donjoy, Inc.
- Product code
- Code HCC
- Device class
- Class 2
- Regulation
- 21 CFR 882.5050
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Carsbad, CA, US
Recent devices under product code HCC
view allMore clearances from Smith and Nephew Donjoy, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.