GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP
FDA 510(k) clearance K897119 · decided 1990-04-12
Clearance details
- K-number
- K897119
- Device name
- GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP
- Applicant
- Grieshaber & Co.
- Decision
- Substantially Equivalent
- Date received
- 1989-12-26
- Decision date
- 1990-04-12
- Days to decision
- 107 days
- Clearance type
- Traditional
- Product code
- HQW
- Device class
- 2
- Regulation number
- 886.3100
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Langhorne, PA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Grieshaber & Co.
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| RETINAL TAAK (K901275) | Alcon Surgical, Inc. | 1990-03-23 |
| DOUBLE & SINGLE TANTALUM CLIPS (K840207) | Storz Instrument Co. | 1984-03-29 |
Recalls involving this device
No recalls on record reference this clearance.