MENTOR HORIZON LOW VISION MAGNIFIER
FDA 510(k) clearance K915340 · decided 1992-03-30
Clearance details
- K-number
- K915340
- Device name
- MENTOR HORIZON LOW VISION MAGNIFIER
- Applicant
- Mentor O & O, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-10-24
- Decision date
- 1992-03-30
- Days to decision
- 158 days
- Clearance type
- Traditional
- Product code
- HJG
- Device class
- 1
- Regulation number
- 886.5820
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Norwell, MA, 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 |
|---|---|---|
| LOW-VISION READING AID, HELPMATE 2020, VISION-AIDE, LV HELPMATE (K933633) | Gracefully Yours, Inc. | 1994-02-22 |
| MAGNI-CAM (K920069) | Innoventions, Inc. | 1992-03-02 |
| MAGNILINK SYSTEM 602 (K892351) | Coburn Optical Ind., Inc. | 1989-05-26 |
| MAGNILINK SYSTEM 101 (K892347) | Coburn Optical Ind., Inc. | 1989-05-26 |
| MAGNILINK SYSTEM 201 (K892348) | Coburn Optical Ind., Inc. | 1989-05-26 |
| MAGNILINK SYSTEM 402/5 (K892350) | Coburn Optical Ind., Inc. | 1989-05-26 |
| MAGNILINK SYSTEM 209 (K892349) | Coburn Optical Ind., Inc. | 1989-05-26 |
Recalls involving this device
No recalls on record reference this clearance.