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
K890925Substantially Equivalent

Manan Bone Marrow Biopsy Needle

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

K890925 is the FDA 510(k) clearance record for MANAN BONE MARROW BIOPSY NEEDLE, a class I device, cleared for Manan Medical Products, Inc. on under FDA product code DWO (Needle, Biopsy, Cardiovascular). FDA records list 64 510(k) clearances for ARGON MEDICAL DEVICES INC., from to . As of , FDA records show 7 recalls naming K890925.

Clearance record

Decision date
Received
(46 days to decision)
Product code
DWO Needle, Biopsy, Cardiovascular
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Manan Medical Products, Inc. 2200 Carlson Dr., Northbrook IL
Third party review
No

Clearances, product code DWO

Trailing 12 months

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

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