510(k) K833006
K833006 is an FDA 510(k) premarket notification submitted by Modern Systems, Inc. for the device "CEPHALOMETER & FIXATOR". The FDA issued a decision of Substantially Equivalent on January 3, 1984. The device falls under product code EAG (Cephalometer), a Class II device regulated under 21 CFR 872.1830.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 3, 1984
- Date Received
- September 6, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cephalometer
- Device Class
- Class II
- Regulation Number
- 872.1830
- Review Panel
- RA
- Submission Type