VASCUTEK GRAFT SIZER SET
FDA 510(k) clearance K955588 · decided 1996-03-07
Clearance details
- K-number
- K955588
- Device name
- VASCUTEK GRAFT SIZER SET
- Applicant
- Carbomedics, Inc.
- Decision
- Substantially Equivalent - Subject to Tracking Reg.
- Date received
- 1995-12-07
- Decision date
- 1996-03-07
- Days to decision
- 91 days
- Clearance type
- Traditional
- Product code
- DSY
- Device class
- 2
- Regulation number
- 870.3450
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Austin, TX, US
- Third-party review
- No
- Expedited review
- No
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| GORE® PROPATEN® Vascular Graft (K240083) | W. L. Gore & Associates, Inc. | 2024-03-01 |
| exGraft ePTFE Vascular Grafts, exGraft Carbon ePTFE Vascular Grafts (K233783) | Peca Labs, Inc. | 2024-01-17 |
| GORE® PROPATEN® Vascular Graft (K232312) | W. L. Gore & Associates, Inc. | 2024-01-09 |
| GORE® ACUSEAL Vascular Graft (K233551) | W. L. Gore & Associates, Inc. | 2023-12-19 |
| GORE® ACUSEAL Vascular Graft (K231505) | W. L. Gore & Associates, Inc. | 2023-06-23 |
| HeRO Graft (K213845) | Merit Medical Systems, Inc. | 2022-08-15 |
| exGraft, exGraft Carbon (K221628) | Peca Labs | 2022-08-04 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| VASCUTEK GELSOFT(TM) VASCULAR GRAFT (P890045/S001) | Carbomedics, Inc. | 1995-07-05 |
| VASCUTEK GELSEAL(TM) VASCULAR GRAFT (P890045/S005) | Carbomedics, Inc. | 1995-04-13 |
| VASCUTEK GELSEAL(TM) VASCULAR GRAFT (P890045/S006) | Carbomedics, Inc. | 1994-07-22 |
| VASCUTEK GELSOFT(TM) VASCULAR GRAFT (P890045/S003) | Carbomedics, Inc. | 1993-12-07 |
| GELSEAL TM TRIAXIAL VASCULAR GRAFT (P890045) | Carbomedics, Inc. | 1993-01-11 |