ERCHONIA IOTO_240— 510(k) K062792
Substantially EquivalentErchonia Medical, Inc.
FDA 510(k) clearance K062792 for ERCHONIA IOTO_240, Substantially Equivalent on 2007-03-01. Applicant: Erchonia Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Erchonia Medical, Inc.
- Product code
- Code EGJ
- Device class
- Class 2
- Regulation
- 21 CFR 890.5525
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Littleton, CO, US
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