510(k) K915005
K915005 is an FDA 510(k) premarket notification submitted by Espe GmbH (Us) for the device "PHOTAC-BOND APLICAP, MODIFICATION". The FDA issued a decision of Substantially Equivalent on January 14, 1992. The device falls under product code EMA (Cement, Dental), a Class II device regulated under 21 CFR 872.3275. Espe GmbH (Us) has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 14, 1992
- Date Received
- November 7, 1991
- 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