510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K983490Substantially Equivalent

Terumo Venoject,luer Adapter

Terumo Corp., Elkton MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K983490 is the FDA 510(k) clearance record for TERUMO VENOJECT,LUER ADAPTER, a class II device, cleared for Terumo Corp. on under FDA product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection). FDA records list 34 510(k) clearances for Terumo Corp., from to . As of , FDA records show no recalls naming K983490.

Clearance record

Decision date
Received
(56 days to decision)
Product code
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation
21 CFR 862.1675
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Terumo Corp. 125 Blue Ball Rd., Elkton MD
510(k) summary
Summary
Third party review
No

Clearances, product code JKA

Trailing 12 months
6 clearances under product code JKA in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code JKA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20263
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260