510(k) K933543
K933543 is an FDA 510(k) premarket notification submitted by Jedental Co., Inc. for the device "ZOE CEMENT (ZINC OXIDE & EUGENOL CEMENT)". The FDA issued a decision of Substantially Equivalent on November 1, 1993. The device falls under product code EMA (Cement, Dental), a Class II device regulated under 21 CFR 872.3275. Jedental Co., Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 1, 1993
- Date Received
- July 20, 1993
- 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