The following data is part of a premarket notification filed by Molded Products Inc. with the FDA for Mpc-1000 Injection Cap/plug.
| Device ID | K925927 |
| 510k Number | K925927 |
| Device Name: | MPC-1000 INJECTION CAP/PLUG |
| Classification | Set, Administration, Intravascular |
| Applicant | MOLDED PRODUCTS INC. 1600 CHATBURN AVE. P.O. BOX 15 Harlan, IA 51537 |
| Contact | Rebecca Will |
| Correspondent | Rebecca Will MOLDED PRODUCTS INC. 1600 CHATBURN AVE. P.O. BOX 15 Harlan, IA 51537 |
| Product Code | FPA |
| CFR Regulation Number | 880.5440 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-11-23 |
| Decision Date | 1993-08-16 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| B144MPC1301 | K925927 | 000 |
| B144MPC1231 | K925927 | 000 |
| B144MPC115LB103 | K925927 | 000 |
| B144MPC115LB503 | K925927 | 000 |
| B144MPC1353 | K925927 | 000 |
| B144MPC1003 | K925927 | 000 |
| B144MPC1101 | K925927 | 000 |
| B144MPC1153 | K925927 | 000 |
| B144MPC115503 | K925927 | 000 |
| B144MPC124B3 | K925927 | 000 |
| B144MPC1251 | K925927 | 000 |
| B144MPC125B3 | K925927 | 000 |
| B144MPC125R3 | K925927 | 000 |
| B144MPC125Y3 | K925927 | 000 |
| B144MPC100S1 | K925927 | 000 |