HOSPIRA PLUM INFUSION SET; HOSPIRA INFUSION SET WITH YELLOW STRIPE TUBING
FDA 510(k) clearance K103224 · decided 2011-01-07
Clearance details
- K-number
- K103224
- Device name
- HOSPIRA PLUM INFUSION SET; HOSPIRA INFUSION SET WITH YELLOW STRIPE TUBING
- Applicant
- Hospira, Inc.
- Decision
- Substantially Equivalent
- Date received
- 2010-11-01
- Decision date
- 2011-01-07
- Days to decision
- 67 days
- Clearance type
- Special
- Product code
- FPA
- Device class
- 2
- Regulation number
- 880.5440
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Lake Forest, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| List No. 14212-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, Non-Vented, 110 I recall (Z-1856-2013) | Hospira Inc. | 2013-08-05 |
| Hospira Primary Microbore Gemstar Split Set, Integral PAV, Yellow Striped Tubing, 110 Inch recall (Z-2027-2011) | Hospira Inc. | 2011-04-19 |
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| DEXTRAN HM 32% HYSTEROSCOPIC DISTENTION MEDIUM (P880028/S008) | Hospira, Inc. | 1999-01-29 |
| DEXTRAN HM 32% HYSTEROSCOPIC DISTENTION MEDIUM (P880028/S007) | Hospira, Inc. | 1996-09-05 |
| DEXTRAN HM 32% HYSTEROSCOPIC DISTENTION MEDIUM (P880028/S006) | Hospira, Inc. | 1996-01-04 |
| DEXTRAN HM 32% HYSTEROSCOPIC DISTENTION MEDIUM (P880028/S003) | Hospira, Inc. | 1995-12-15 |
| DEXTRAN HM 32 (P880028/S002) | Hospira, Inc. | 1990-11-15 |
| DEXTRAN HM 32 (P880028/S001) | Hospira, Inc. | 1989-12-29 |
| DEXTRAN HM 32% (P880028) | Hospira, Inc. | 1989-05-30 |