GS 3000— 510(k) K102202
Substantially EquivalentEmsi
FDA 510(k) clearance K102202 for GS 3000, Substantially Equivalent on 2010-11-23. Applicant: Emsi. Device class: 2.
Clearance details
- Applicant
- Emsi
- 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
- Alexandria, VA, US
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