510(k) K933455
K933455 is an FDA 510(k) premarket notification submitted by Schick Technologies, Inc. for the device "COMPUTED ORAL RADIOLOGY SYSTEM". The FDA issued a decision of Substantially Equivalent on January 31, 1994. The device falls under product code EAP (Unit, X-Ray, Intraoral), a Class II device regulated under 21 CFR 872.1810. Schick Technologies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 31, 1994
- Date Received
- July 14, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, X-Ray, Intraoral
- Device Class
- Class II
- Regulation Number
- 872.1810
- Review Panel
- RA
- Submission Type