STAPLE REMOVAL KIT
FDA 510(k) clearance K963234 · decided 1996-10-21
Clearance details
- K-number
- K963234
- Device name
- STAPLE REMOVAL KIT
- Applicant
- Continental Medical Laboratories, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1996-08-19
- Decision date
- 1996-10-21
- Days to decision
- 63 days
- Clearance type
- Traditional
- Product code
- GDT
- Device class
- 1
- Regulation number
- 878.4760
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Waterford, WI, 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 |
|---|---|---|
| VISISTAT STAPLER (K943719) | Pilling Weck, Inc. | 1994-08-24 |
| MANIPLER DISPOSABLE SKIN STAPLER (K925526) | Matsutani Seisakusho Co. , Ltd. | 1993-06-24 |
| SKIN STAPLE REMOVER KIT (K915430) | Cypress Medical Products, Ltd. | 1992-02-28 |
| QUALTEX SKIN STAPLE EXTRACTOR (K911204) | Deroyal Industries, Inc. | 1991-05-08 |
| AUTO SUTURE(R) POLYMER SKIN GRAFT STAPLER* (K910586) | United States Surgical, A Division of Tyco Healthc | 1991-03-07 |
| APPOSE UNITY STERILE DISPOSABLE SKIN STAPLER (K900486) | Davis & Geck, Inc. | 1990-04-20 |
| SKIN STAPLE REMOVER WITH SPONGE STERILE DISPOSABLE (K861711) | Busse Hospital Disposables, Inc. | 1986-05-16 |
| V. MUELLER VITAL SKIN STAPLER (K851974) | American V. Mueller | 1985-06-11 |
| SKIN STAT II SKIN STAPLING MEDICAL DEVICE (K844838) | Edward Weck, Inc. | 1985-01-23 |
| VISISTAT SKIN STAPLING DEVICE (K844837) | Edward Weck, Inc. | 1985-01-23 |
| STAPLE REMOVER SR300P (K833085) | Prosper, Inc. | 1984-12-14 |
| VYDAX 525-550 & 5100 FLUOROTELOMER (K833357) | ETHICON, Inc. | 1983-12-12 |
Recalls involving this device
No recalls on record reference this clearance.