WELCH ALLYN GLAUCOMA DETECTOR
FDA 510(k) clearance K941723 · decided 1994-06-06
Clearance details
- K-number
- K941723
- Device name
- WELCH ALLYN GLAUCOMA DETECTOR
- Applicant
- Welch Allyn, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1994-04-07
- Decision date
- 1994-06-06
- Days to decision
- 60 days
- Clearance type
- Traditional
- Product code
- HOO
- Device class
- 1
- Regulation number
- 886.1605
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Skaneateles Falls, NY, 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 |
|---|---|---|
| MARCO PROJECTION PERIMETER (K930448) | Marco Ophthalmic, Inc. | 1993-06-21 |
| RICHMOND VISUAL FIELD SCREENER (K873912) | Richmond Products, Inc. | 1987-11-02 |
| HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREEN (K864467) | Keeler Instruments, Inc. | 1986-12-15 |
| DIGILAB CAMBRIDGE PERIMETER (K860115) | Bio-Rad | 1986-02-27 |
| AUTOMATIC TANGENT SCREEN 50 (K832800) | CooperVision, Inc. | 1983-09-29 |
Recalls involving this device
No recalls on record reference this clearance.