MPC-1000 INJECTION CAP/PLUG
FDA 510(k) clearance K925927 · decided 1993-08-16
Clearance details
- K-number
- K925927
- Device name
- MPC-1000 INJECTION CAP/PLUG
- Applicant
- Molded Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1992-11-23
- Decision date
- 1993-08-16
- Days to decision
- 266 days
- Clearance type
- Traditional
- Product code
- FPA
- Device class
- 2
- Regulation number
- 880.5440
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Harlan, IA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| See Luer Cap Set, MPC-130, set, administration, intravascular recall (Z-1774-2026) | Molded Products Inc | 2026-04-06 |