ABREU, MODEL 700
FDA 510(k) clearance K100843 · decided 2010-08-17
Clearance details
- K-number
- K100843
- Device name
- ABREU, MODEL 700
- Applicant
- Brain Tunnelgenix Technologies Corp
- Decision
- Substantially Equivalent
- Date received
- 2010-03-25
- Decision date
- 2010-08-17
- Days to decision
- 145 days
- Clearance type
- Traditional
- Product code
- FLL
- Device class
- 2
- Regulation number
- 880.2910
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Naples, FL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Brain Tunnelgenix Technologies Corp
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.