510(k) K993556
K993556 is an FDA 510(k) premarket notification submitted by Medlogic Global Corp. for the device "LIQUIBAND DENTAL". The FDA issued a decision of Substantially Equivalent on January 3, 2000. The device falls under product code EMA (Cement, Dental), a Class II device regulated under 21 CFR 872.3275. Medlogic Global Corp. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 3, 2000
- Date Received
- October 20, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cement, Dental
- Device Class
- Class II
- Regulation Number
- 872.3275
- Review Panel
- DE
- Submission Type