LEUKOCLIP(R)
FDA 510(k) clearance K873744 · decided 1987-09-30
Clearance details
- K-number
- K873744
- Device name
- LEUKOCLIP(R)
- Applicant
- Beiersdorf, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-09-16
- Decision date
- 1987-09-30
- Days to decision
- 14 days
- Clearance type
- Traditional
- Product code
- FZQ
- Device class
- 1
- Regulation number
- 878.4320
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Norwalk, CT, 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 |
|---|---|---|
| RANEY CLIP (K884783) | Alto Development Corp. | 1988-11-30 |
| ONE TIME DISPOSABLE SKIN STAPLER (K830704) | Acme United Corp. | 1983-04-12 |
| DISPOSABLE SKIN STAPLER (K830768) | Surgeons Choice, Inc. | 1983-04-12 |
| SURGICAL PRODUCTS, SKIN STAPLE REMOVER (K822963) | Temp-Stik Corp. | 1982-11-08 |
| COMPLETE (K822145) | Richard-Allan Medical Ind., Inc. | 1982-10-22 |
Recalls involving this device
No recalls on record reference this clearance.