510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K003712Substantially Equivalent

Modification to Male to Male Luer Adapter

Molded Products Inc, Harlan IA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K003712 is the FDA 510(k) clearance record for MODIFICATION TO MALE TO MALE LUER ADAPTER, a class II device, cleared for Molded Products, Inc. on under FDA product code KOC (Accessories, Blood Circuit, Hemodialysis). FDA records list 7 510(k) clearances for Molded Products, Inc., from to . As of , FDA records show 2 recalls naming K003712.

Clearance record

Decision date
Received
(166 days to decision)
Product code
KOC Accessories, Blood Circuit, Hemodialysis
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Molded Products, Inc. P.O. Box 15, Harlan IA
510(k) summary
Statement
Third party review
No

Clearances, product code KOC

Trailing 12 months

FDA records hold no clearances under product code KOC in the trailing twelve months.

FDA records show no clearances under product code KOC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KOC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260