510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K941814Substantially Equivalent

Argyle Dual Lumen Umbilical Vessel Catheter

Sherwood Medical Co., St. Louis MO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K941814 is the FDA 510(k) clearance record for ARGYLE DUAL LUMEN UMBILICAL VESSEL CATHETER, a class II device, cleared for Sherwood Medical Co. on under FDA product code FOS (Catheter, Umbilical Artery). FDA records list 191 510(k) clearances for Sherwood Medical Co., from to . As of , FDA records show one recall naming K941814.

Clearance record

Decision date
Received
(171 days to decision)
Product code
FOS Catheter, Umbilical Artery
Regulation
21 CFR 880.5200
Device class
Class II
Review panel
General Hospital
Applicant
Sherwood Medical Co. 1915 Olive St., St. Louis MO
510(k) summary
Summary
Third party review
No

Clearances, product code FOS

Trailing 12 months

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

FDA records show no clearances under product code FOS in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FOS, 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