Company ยท US
Molded Products, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1993 to 2002. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
4recalls (1 in 12 months)
4recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 23, 2002 | K022068 | TUBING, DIALYSATE (AND CONNECTOR) Molded Products, Inc. | FID |
| Nov 28, 2001 | K010366 | DISPOSABLE STORAGE CAP Molded Products, Inc. | FJI |
| Sep 27, 2001 | K010712 | DIALYSATE LINE WITH CONNECTORS/RE-USE WASH-OUT LINES Molded Products, Inc. | FID |
| May 16, 2001 | K003712 | MODIFICATION TO MALE TO MALE LUER ADAPTER Molded Products, Inc. | KOC |
| Jan 14, 1994 | K925978 | MPC-80 TRANSDUCER Molded Products, Inc. | FIB |
| Aug 16, 1993 | K925930 | MPC-150 MALE TO MALE LUER ADAPTER Molded Products, Inc. | FPA |
| Aug 16, 1993 | K925927 | MPC-1000 INJECTION CAP/PLUG Molded Products, Inc. | FPA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 6, 2026 | Molded Products Inc See Luer Cap Set, MPC-130, set, administration, intravascular Open, Classified |
FPA | K925927 |
| Jun 10, 2019 | Molded Products Inc Luer Lock Set - Catalog # MPC-125, for IV administration sets. Terminated |
FPA | K925927 |
| Mar 24, 2017 | Molded Products Inc Non-Sterile Double DIN to DIN "Y" Connector,
Product Usage:
Extension for connecting hemodialysis blood tubing to the hemodialyzer. Terminated |
KOC | K003712 |
| Mar 18, 2013 | Molded Products Inc Sterile Access & Return Line Set, 36" Length, Part # UM-872-36.
Intended for use with medically prescribed hemodialysis blood tubing. Terminated |
KOC | K003712 |