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
K993442Substantially Equivalent

Vygon Lifecath-Picc (Pur) Catheters (Single and Double Lumen 3Fr, 4Fr, 4.5Fr, and 5Fr)

Vygon Corp., West Cadwell NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K993442 is the FDA 510(k) clearance record for VYGON LIFECATH-PICC (PUR) CATHETERS (SINGLE AND DOUBLE LUMEN 3FR, 4FR, 4.5FR, AND 5FR), a class II device, cleared for Vygon Corp. on under FDA product code LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days). FDA records list 11 510(k) clearances for Vygon Corp., from to . As of , FDA records show no recalls naming K993442.

Clearance record

Decision date
Received
(296 days to decision)
Product code
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Regulation
21 CFR 880.5970
Device class
Class II
Review panel
General Hospital
Applicant
Vygon Corp. 1129 Bloomfield Ave., West Cadwell NJ
510(k) summary
Statement
Third party review
No

Clearances, product code LJS

Trailing 12 months
3 clearances under product code LJS in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LJS, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260