LHO — Instrument, Quality-Assurance, Radiologic Class I
FDA Device Classification
Classification Details
- Product Code
- LHO
- Device Class
- Class I
- Regulation Number
- 892.1940
- Submission Type
- Review Panel
- RA
- Medical Specialty
- Radiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K042733 | standard imaging | STANDARD IMAGING PIPSPRO QA SOFTWARE SYSTEM | November 15, 2004 |
| K873956 | radiation measurements | ULTIMETER | October 30, 1987 |
| K853754 | victoreen | MAGNETIC RESONANCE IMAGING UNIFORMITY/T1 76-901 | May 7, 1986 |
| K860260 | victoreen | MULTI PURPOSE MODEL 76-903 | May 7, 1986 |
| K860100 | victoreen | MRI SLICE THICKNESS & CONTIGUITY PHANTOM #76-902 | April 22, 1986 |
| K844620 | varian assoc | BDS-3 BEAM DATA SCANNER | July 1, 1985 |
| K845007 | varian assoc | RFA-7 RADIATION FIELD ANALYZER | July 1, 1985 |
| K834483 | radiation measurements | DIGI-X | March 5, 1984 |