USCI ILLUMEN-8 8F PTCA GUIDING CATHETER
FDA 510(k) clearance K910154 · decided 1991-04-09
Clearance details
- K-number
- K910154
- Device name
- USCI ILLUMEN-8 8F PTCA GUIDING CATHETER
- Applicant
- C.R. Bard, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-01-14
- Decision date
- 1991-04-09
- Days to decision
- 85 days
- Clearance type
- Traditional
- Product code
- DOY
- Device class
- 2
- Regulation number
- 862.3320
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- Billerica, MA, 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 |
|---|---|---|
| CENTRAL VENOUS ACCESS CATHETER CVAC (K832396) | Gish Biomedical, Inc. | 1983-08-31 |
| WALRUS PERCUTANEOUS INTRODUCER SET (K831239) | Medical Parameters, Inc. | 1983-05-25 |
| VASCULAR CATHETER (K831191) | Medrad, Inc. | 1983-05-09 |
| CONNECTOR TUBE (K831188) | Medrad, Inc. | 1983-05-09 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| Covera Vascular Covered Stent (P170042/S014) | C.R. Bard, Inc. | 2025-12-16 |
| Covera Vascular Covered Stents (P170042/S013) | C.R. Bard, Inc. | 2025-06-26 |
| Avitene Microfibrillar Collagen Hemostat (P800002/S033) | C.R. Bard, Inc. | 2025-03-13 |
| AVITENE MICROFIBRILLAR COLLAGEN HEMOSTAT NON-WOVEN WEB (P800002/S032) | C.R. Bard, Inc. | 2025-02-18 |
| Avitene Bulk Flour Cleanroom Expansion (P800002/S031) | C.R. Bard, Inc. | 2024-01-18 |
| Avitene Microfibrillar Collagen Hemostat (P800002/S030) | C.R. Bard, Inc. | 2023-10-04 |
| Covera Vascular Covered Stent (P170042/S012) | C.R. Bard, Inc. | 2023-02-02 |
| Avitene Microfibrillar Collagen Hemostat (MCH) Non-Woven Web and Avitene Microfibrillar Collagen Hemostat (MCH) EndoAvit (P800002/S027) | C.R. Bard, Inc. | 2022-04-01 |