BARD REPLACEMENT GASTROSTOMY TUBE
FDA 510(k) clearance K910492 · decided 1991-07-24
Clearance details
- K-number
- K910492
- Device name
- BARD REPLACEMENT GASTROSTOMY TUBE
- Applicant
- C.R. Bard, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1991-02-05
- Decision date
- 1991-07-24
- Days to decision
- 169 days
- Clearance type
- Traditional
- Product code
- KGC
- Device class
- 2
- Regulation number
- 876.5980
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Murray Hill, NJ, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| 18F Tri-Funnel Replacement Gastrostomy Tube recall (Z-0836-06) | Bard Access Systems, Inc | 2006-05-03 |
| 20F Tri-Funnel Replacement Gastrostomy Tube recall (Z-0837-06) | Bard Access Systems, Inc | 2006-05-03 |
| 22F Tri-Funnel Replacement Gastrostomy Tube recall (Z-0838-06) | Bard Access Systems, Inc | 2006-05-03 |
| 24F Tri-Funnel Replacement Gastrostomy Tube recall (Z-0839-06) | Bard Access Systems, Inc | 2006-05-03 |
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 |