FTZ — Locator, Magnetic Class I
FDA Device Classification
Classification Details
- Product Code
- FTZ
- Device Class
- Class I
- Regulation Number
- 886.4445
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K833229 | h and m douglas enterprises | SUN BED BY VERRE ET QUARTZ UVA-FRANCE | January 27, 1984 |
| K830468 | western laboratories | MODEL 200 | April 12, 1983 |