510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K232316Substantially Equivalent

DEKA Infusion System, DEKA Administration Set

Deka Research & Development Corp., Manchester NH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K232316 is the FDA 510(k) clearance record for DEKA Infusion System, DEKA Administration Set, a class II device, cleared for Deka Research and Development on under FDA product code LDR (Controller, Infusion, Intravascular, Electronic). FDA records list 28 510(k) clearances for Deka Research and Development, from to . As of , FDA records show no recalls naming K232316.

Clearance record

Decision date
Received
(211 days to decision)
Product code
LDR Controller, Infusion, Intravascular, Electronic
Regulation
21 CFR 880.5725
Device class
Class II
Review panel
General Hospital
Applicant
Deka Research and Development 340 Commercial St., Manchester NH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LDR

Trailing 12 months

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

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