MPC-1000 INJECTION CAP/PLUG

Set, Administration, Intravascular

MOLDED PRODUCTS INC.

The following data is part of a premarket notification filed by Molded Products Inc. with the FDA for Mpc-1000 Injection Cap/plug.

Pre-market Notification Details

Device IDK925927
510k NumberK925927
Device Name:MPC-1000 INJECTION CAP/PLUG
ClassificationSet, Administration, Intravascular
Applicant MOLDED PRODUCTS INC. 1600 CHATBURN AVE. P.O. BOX 15 Harlan,  IA  51537
ContactRebecca Will
CorrespondentRebecca Will
MOLDED PRODUCTS INC. 1600 CHATBURN AVE. P.O. BOX 15 Harlan,  IA  51537
Product CodeFPA  
CFR Regulation Number880.5440 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-11-23
Decision Date1993-08-16

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
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

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