CORFLO 300 PUMP
FDA 510(k) clearance K944750 · decided 1995-06-19
Clearance details
- K-number
- K944750
- Device name
- CORFLO 300 PUMP
- Applicant
- Corpak, Inc.
- Decision
- Substantially Equivalent - Subject to Tracking & PMS
- Date received
- 1994-09-26
- Decision date
- 1995-06-19
- Days to decision
- 266 days
- Clearance type
- Traditional
- Product code
- FRN
- Device class
- 2
- Regulation number
- 880.5725
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Wheeling, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| CORFLO 300 Enteral Pump; a volumetric rotary peristaltic intermittent enteral feeding pump recall (Z-0089-2012) | CORPAK MedSystems | 2011-10-25 |