GUIDOSS
FDA 510(k) clearance K133507 · decided 2014-11-05
Clearance details
- K-number
- K133507
- Device name
- GUIDOSS
- Applicant
- Nibec Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2013-11-14
- Decision date
- 2014-11-05
- Days to decision
- 356 days
- Clearance type
- Traditional
- Product code
- NPL
- Device class
- 2
- Regulation number
- 872.3930
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Los Angeles, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.