510(k) K070114
K070114 is an FDA 510(k) premarket notification submitted by Jensen Industries, Inc. for the device "CREATION CP-ZI PORCELAIN". The FDA issued a decision of Substantially Equivalent on March 1, 2007. The device falls under product code EIH (Powder, Porcelain), a Class II device regulated under 21 CFR 872.6660. Jensen Industries, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 1, 2007
- Date Received
- January 12, 2007
- Clearance Type
- Abbreviated
- 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