510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K950861Substantially Equivalent

Reconstitution Accessoreis

Organon LLC, West Orange NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K950861 is the FDA 510(k) clearance record for RECONSTITUTION ACCESSOREIS, a class II device, cleared for Organon, Inc. on under FDA product code FPK (Tubing, Fluid Delivery). FDA records list 42 510(k) clearances for Organon, Inc., from to . As of , FDA records show no recalls naming K950861.

Clearance record

Decision date
Received
(88 days to decision)
Product code
FPK Tubing, Fluid Delivery
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Organon, Inc. 375 Mount Pleasant Ave., West Orange NJ
510(k) summary
Summary
Third party review
No

Clearances, product code FPK

Trailing 12 months

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

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