RELIEVA LUMA SINUS ILLUMINATION SYSTEM, MODEL SIS-100A— 510(k) K071845
Substantially EquivalentAcclarent, Inc.
FDA 510(k) clearance K071845 for RELIEVA LUMA SINUS ILLUMINATION SYSTEM, MODEL SIS-100A, Substantially Equivalent on 2007-09-28. Applicant: Acclarent, Inc.. Device class: 1.
Clearance details
- Applicant
- Acclarent, Inc.
- Product code
- Code KAM
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rmenlo Park, CA, US
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