SOPIX 2
FDA 510(k) clearance K092329 · decided 2010-07-20
Clearance details
- K-number
- K092329
- Device name
- SOPIX 2
- Applicant
- Sopro
- Decision
- Substantially Equivalent
- Date received
- 2009-08-04
- Decision date
- 2010-07-20
- Days to decision
- 350 days
- Clearance type
- Traditional
- Product code
- MUH
- Device class
- 2
- Regulation number
- 872.1800
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Mt. Laurel, NJ, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Sopro
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.