510(k) K895085
K895085 is an FDA 510(k) premarket notification submitted by Lustgarten Multi-Tech International, Inc. for the device "WALKLITE PROTABLE RE-CHARGEABLE CURING LIGHT". The FDA issued a decision of Substantially Equivalent on April 2, 1990. The device falls under product code EBZ (Activator, Ultraviolet, For Polymerization), a Class II device regulated under 21 CFR 872.6070. Lustgarten Multi-Tech International, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 2, 1990
- Date Received
- August 14, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Activator, Ultraviolet, For Polymerization
- Device Class
- Class II
- Regulation Number
- 872.6070
- Review Panel
- DE
- Submission Type