LQA — Media, Reusable Image Class I
FDA product code LQA covers "Media, Reusable Image", a Class I medical device regulated under 21 CFR 892.1840. Submissions are reviewed by the Radiology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LQA
- Device Class
- Class I
- Regulation Number
- 892.1840
- Submission Type
- Review Panel
- RA
- Medical Specialty
- Radiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K854407 | digirad | DIGIRAD REUSABLE IMAGE MEDIA | March 10, 1986 |