IYP — Phantom, Anthropomorphic, Nuclear Class I
FDA Device Classification
Classification Details
- Product Code
- IYP
- Device Class
- Class I
- Regulation Number
- 892.1370
- Submission Type
- Review Panel
- RA
- Medical Specialty
- Radiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K921878 | circadian | SCANMATE III | September 11, 1992 |
| K844189 | elscint | LINEAR SCANNER PROBE ELSCINT LTD. TL-35 | February 25, 1985 |
| K812893 | mick radio-nuclear instruments | SUPERFLAB | December 8, 1981 |