510(k) K160144
K160144 is an FDA 510(k) premarket notification submitted by Genoss Co., Ltd. for the device "rainbow LS Block". The FDA issued a decision of Substantially Equivalent on July 21, 2016. The device falls under product code EIH (Powder, Porcelain), a Class II device regulated under 21 CFR 872.6660. Genoss Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 21, 2016
- Date Received
- January 21, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Powder, Porcelain
- Device Class
- Class II
- Regulation Number
- 872.6660
- Review Panel
- DE
- Submission Type