MOSAIC LASER SYSTEM
FDA 510(k) clearance K080932 · decided 2008-06-09
Clearance details
- K-number
- K080932
- Device name
- MOSAIC LASER SYSTEM
- Applicant
- Lutronic Corporation
- Decision
- Substantially Equivalent
- Date received
- 2008-04-02
- Decision date
- 2008-06-09
- Days to decision
- 68 days
- Clearance type
- Special
- Product code
- GEX
- Device class
- 2
- Regulation number
- 878.4810
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- North Reading, MA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Lutronic Corporation
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.