FT2000 SEQUENCER FOR MUSCLE STIMULATOR— 510(k) K050595
Substantially EquivalentMidwest Development
FDA 510(k) clearance K050595 for FT2000 SEQUENCER FOR MUSCLE STIMULATOR, Substantially Equivalent on 2005-05-23. Applicant: Midwest Development. Device class: 2.
Clearance details
- Applicant
- Midwest Development
- 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
- Egale, WI, US
Recent devices under product code IPF
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