510(k) K050362
K050362 is an FDA 510(k) premarket notification submitted by Vident for the device "VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)". The FDA issued a decision of Substantially Equivalent on Mar 15, 2005. The device falls under product code EIH (Powder, Porcelain), a Class II device regulated under 21 CFR 872.6660. Vident has 35 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 15, 2005
- Date Received
- Feb 14, 2005
- 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
- 510(k)