Device |
densitometer, bone |
Regulation Description |
Bone densitometer. |
Regulation Medical Specialty |
Radiology |
Review Panel |
Radiology |
Product Code | KGI |
Premarket Review |
Office of Radiological Health
(OHT8)
Radiological Imaging Devices and Electronic Products
(DHT8B)
|
Submission Type |
510(k)
|
Regulation Number |
892.1170
|
Device Class |
2
|
Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
GMP Exempt? |
No
|
Summary Malfunction Reporting |
Eligible |
Implanted Device? |
No
|
Life-Sustain/Support Device? |
No
|
Guidance Document
|
Third Party Review
|
Accredited Persons
|
|
|