RETINAL TAAK
FDA 510(k) clearance K901275 · decided 1990-03-23
Clearance details
- K-number
- K901275
- Device name
- RETINAL TAAK
- Applicant
- Alcon Surgical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1990-03-19
- Decision date
- 1990-03-23
- Days to decision
- 4 days
- Clearance type
- Traditional
- Product code
- HQW
- Device class
- 2
- Regulation number
- 886.3100
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Irvine, CA, 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 |
|---|---|---|
| GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP (K897119) | Grieshaber & Co. | 1990-04-12 |
| DOUBLE & SINGLE TANTALUM CLIPS (K840207) | Storz Instrument Co. | 1984-03-29 |
Recalls involving this device
No recalls on record reference this clearance.