ADHEAR System
FDA 510(k) clearance K172460 · decided 2018-04-27
Clearance details
- K-number
- K172460
- Device name
- ADHEAR System
- Applicant
- Med-El Elektromedizinische Geraete GmbH
- Decision
- Substantially Equivalent
- Date received
- 2017-08-14
- Decision date
- 2018-04-27
- Days to decision
- 256 days
- Clearance type
- Traditional
- Product code
- LXB
- Device class
- 2
- Regulation number
- 874.3302
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- Location
- Innsbruck, AT
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.