510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930218Substantially Equivalent

Subcutaneous Tunneling Needle and Handles

Concord/Portex, Keene NH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930218 is the FDA 510(k) clearance record for SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES, a class II device, cleared for Concord/Portex on under FDA product code MAJ (Catheter, Percutaneous, Intraspinal, Short Term). FDA records list 23 510(k) clearances for Concord/Portex, from to . As of , FDA records show no recalls naming K930218.

Clearance record

Decision date
Received
(193 days to decision)
Product code
MAJ Catheter, Percutaneous, Intraspinal, Short Term
Regulation
21 CFR 868.5120
Device class
Class II
Review panel
Anesthesiology
Applicant
Concord/Portex 15 Kitt St., Keene NH
510(k) summary
Summary
Third party review
No

Clearances, product code MAJ

Trailing 12 months

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

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