NORODYN 8000 SEMG SYSTEM, ND-8000— 510(k) K992439
Substantially EquivalentMyotronics-Noromed, Inc.
FDA 510(k) clearance K992439 for NORODYN 8000 SEMG SYSTEM, ND-8000, Substantially Equivalent on 1999-08-13. Applicant: Myotronics-Noromed, Inc.. Device class: 2.
Clearance details
- Applicant
- Myotronics-Noromed, 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
- Special
- Location
- Tukwila, WA, US
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