ULTRA WAVE 101— 510(k) K905836
Substantially EquivalentAko USA, Inc.
FDA 510(k) clearance K905836 for ULTRA WAVE 101, Substantially Equivalent on 1991-01-14. Applicant: Ako USA, Inc.. Device class: 1.
Clearance details
- Applicant
- Ako USA, Inc.
- Product code
- Code IRO
- Device class
- Class 1
- Regulation
- 21 CFR 890.5975
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irving, TX, US
Recent devices under product code IRO
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