510(k) K902972
K902972 is an FDA 510(k) premarket notification submitted by Cmp Industries, LLC for the device "FLEXOR (DENTURE ACRYLIC RELINE MATERIAL)". The FDA issued a decision of Substantially Equivalent on October 4, 1990. The device falls under product code EBI (Resin, Denture, Relining, Repairing, Rebasing), a Class II device regulated under 21 CFR 872.3760. Cmp Industries, LLC has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 4, 1990
- Date Received
- July 6, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Resin, Denture, Relining, Repairing, Rebasing
- Device Class
- Class II
- Regulation Number
- 872.3760
- Review Panel
- DE
- Submission Type