510(k) K780834
K780834 is an FDA 510(k) premarket notification submitted by Hoyt Laboratories for the device "PREVI DENT PROPHYLAXIS MINT NDC". The FDA issued a decision of Substantially Equivalent on June 2, 1978. The device falls under product code EJR (Agent, Polishing, Abrasive, Oral Cavity), a Class I device regulated under 21 CFR 872.6030. Hoyt Laboratories has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 2, 1978
- Date Received
- May 24, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Agent, Polishing, Abrasive, Oral Cavity
- Device Class
- Class I
- Regulation Number
- 872.6030
- Review Panel
- DE
- Submission Type