510(k) K122016
K122016 is an FDA 510(k) premarket notification submitted by Meta Biomed, Inc. for the device "REXTAR, REXTAR LCD". The FDA issued a decision of Substantially Equivalent on Mar 1, 2013. The device falls under product code EHD (Unit, X-Ray, Extraoral With Timer), a Class II device regulated under 21 CFR 872.1800. Meta Biomed, Inc. has 3 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 1, 2013
- Date Received
- Jul 10, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Unit, X-Ray, Extraoral With Timer
- Device Class
- Class II
- Regulation Number
- 872.1800
- Review Panel
- RA
- Submission Type
- 510(k)