The following data is part of a premarket notification filed by Sirona Dental Systems Gmbh with the FDA for Orthophos Ds/dc Ceph, Orthophos 5/plus/cd.
Device ID | K013650 |
510k Number | K013650 |
Device Name: | ORTHOPHOS DS/DC CEPH, ORTHOPHOS 5/PLUS/CD |
Classification | System, X-ray, Extraoral Source, Digital |
Applicant | SIRONA DENTAL SYSTEMS GMBH 49 PLAIN ST. North Attleboro, MA 02760 -4153 |
Contact | Sheila M Hemeon-heyer |
Correspondent | Sheila M Hemeon-heyer SIRONA DENTAL SYSTEMS GMBH 49 PLAIN ST. North Attleboro, MA 02760 -4153 |
Product Code | MUH |
CFR Regulation Number | 872.1800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-11-06 |
Decision Date | 2001-12-06 |
Summary: | summary |