KYD — Strip, Schirmer Class I
FDA Device Classification
Classification Details
- Product Code
- KYD
- Device Class
- Class I
- Regulation Number
- 886.1800
- Submission Type
- Review Panel
- OP
- Medical Specialty
- Ophthalmic
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K911734 | northland cataract and eye care clinic | TEARTEC RAPID LACRIMAL ASSESMENT SYSTEM | November 7, 1991 |
| K881515 | visionex | TEAR VOLUME TESTS | May 23, 1988 |
| K832181 | smith and nephew | SNO STRIPS STERILE TEARFLOW TEST STRIP | August 12, 1983 |