510(k) K040672
K040672 is an FDA 510(k) premarket notification submitted by Wieland Dental + Technik GmbH & Co. KG for the device "PORTA REFLEX". The FDA issued a decision of Substantially Equivalent on May 27, 2004. The device falls under product code EJT (Alloy, Gold-Based Noble Metal), a Class II device regulated under 21 CFR 872.3060. Wieland Dental + Technik GmbH & Co. KG has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 27, 2004
- Date Received
- March 15, 2004
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Alloy, Gold-Based Noble Metal
- Device Class
- Class II
- Regulation Number
- 872.3060
- Review Panel
- DE
- Submission Type