510(k) K872943
K872943 is an FDA 510(k) premarket notification submitted by Dentsply Intl. for the device "DISPOSABLE ARTICULATOR". The FDA issued a decision of Substantially Equivalent on August 11, 1987. The device falls under product code EJP (Articulators), a Class I device regulated under 21 CFR 872.3150. Dentsply Intl. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 11, 1987
- Date Received
- July 28, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Articulators
- Device Class
- Class I
- Regulation Number
- 872.3150
- Review Panel
- DE
- Submission Type