TANGENT SCREEN
FDA 510(k) clearance K873919 · decided 1987-10-28
Clearance details
- K-number
- K873919
- Device name
- TANGENT SCREEN
- Applicant
- Richmond Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-09-25
- Decision date
- 1987-10-28
- Days to decision
- 33 days
- Clearance type
- Traditional
- Product code
- HOJ
- Device class
- 1
- Regulation number
- 886.1810
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Boca Raton, FL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| SPECTABLE FRAME MAGNIFYING BRILLETTE (K844657) | Pro Design Intl. AS | 1984-12-11 |
| CHART PROJECTOR (K821081) | Medical Equipment Designs, Inc. | 1982-06-14 |
Recalls involving this device
No recalls on record reference this clearance.