BURTON AUTOMATIC PROJECTOR - MODEL CP-40
FDA 510(k) clearance K924774 · decided 1993-04-14
Clearance details
- K-number
- K924774
- Device name
- BURTON AUTOMATIC PROJECTOR - MODEL CP-40
- Applicant
- R.H. Burton Co.
- Decision
- Substantially Equivalent
- Date received
- 1992-09-23
- Decision date
- 1993-04-14
- Days to decision
- 203 days
- Clearance type
- Traditional
- Product code
- HOD
- Device class
- 1
- Regulation number
- 886.4350
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Grove City, OH, US
- Third-party review
- No
- Expedited review
- No
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|---|---|---|
| HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER (K891610) | Keeler Instruments, Inc. | 1989-06-05 |
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Recalls involving this device
No recalls on record reference this clearance.