DentureID Microchip
FDA 510(k) clearance K170423 · decided 2017-10-25
Clearance details
- K-number
- K170423
- Device name
- DentureID Microchip
- Applicant
- Cmp Industries, LLC
- Decision
- Substantially Equivalent
- Date received
- 2017-02-13
- Decision date
- 2017-10-25
- Days to decision
- 254 days
- Clearance type
- Traditional
- Product code
- PYQ
- Device class
- 2
- Regulation number
- 880.6300
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Albany, NY, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Cmp Industries
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.
Recalls involving this device
No recalls on record reference this clearance.