510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K883744Substantially Equivalent

Manan Huber Style Infusion Needle

Argon Medical Devices, Inc, Skokie IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883744 is the FDA 510(k) clearance record for MANAN HUBER STYLE INFUSION NEEDLE, a class II device, cleared for Manan Medical Products, Inc. on under FDA product code FMF (Syringe, Piston). FDA records list 64 510(k) clearances for ARGON MEDICAL DEVICES INC., from to . As of , FDA records show no recalls naming K883744.

Clearance record

Decision date
Received
(27 days to decision)
Product code
FMF Syringe, Piston
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Applicant
Manan Medical Products, Inc. 8020 N. Central Park Ave., Skokie IL
Third party review
No

Clearances, product code FMF

Trailing 12 months
14 clearances under product code FMF in the twelve months to October 2026, December 2025 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code FMF, trailing twelve months
MonthClearances
November 20251
December 20254
January 20260
February 20261
March 20260
April 20261
May 20261
June 20262
July 20261
August 20263
September 20260
October 20260