510(k) K992896
K992896 is an FDA 510(k) premarket notification submitted by Dental X-Ray Support Systems, Inc. for the device "DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830)". The FDA issued a decision of Substantially Equivalent on September 3, 1999. The device falls under product code EGY (Processor, Radiographic-Film, Automatic, Dental), a Class II device regulated under 21 CFR 892.1900.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 3, 1999
- Date Received
- August 27, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Processor, Radiographic-Film, Automatic, Dental
- Device Class
- Class II
- Regulation Number
- 892.1900
- Review Panel
- RA
- Submission Type