SELITHERM, MODEL C100— 510(k) K030382
Substantially EquivalentSelicor, Inc.
FDA 510(k) clearance K030382 for SELITHERM, MODEL C100, Substantially Equivalent on 2003-04-01. Applicant: Selicor, Inc.. Device class: 2.
Clearance details
- Applicant
- Selicor, Inc.
- Product code
- Code IMJ
- Device class
- Class 2
- Regulation
- 21 CFR 890.5290
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Austin, TX, US
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