Cleared Traditional

K950861 - RECONSTITUTION ACCESSOREIS

K950861 is an FDA 510(k) clearance for RECONSTITUTION ACCESSOREIS, manufactured by Organon, Inc.. The device is a Class 2 General Hospital device with product code FPK cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K950861 · Organon, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1995
Decision
88d
Days
Class 2
Risk

K950861 is an FDA 510(k) clearance for the RECONSTITUTION ACCESSOREIS. Classified as Tubing, Fluid Delivery (product code FPK), Class II - Special Controls.

Submitted by Organon, Inc. (West Orange, US). The FDA issued a Cleared decision on May 26, 1995 after a review of 88 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5440 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Organon, Inc. devices

FDA 510(k) Submission Details - K950861

510(k) Number K950861 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 27, 1995
Decision Date May 26, 1995
Days to Decision 88 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 129d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FPK Device Classification - Class 2, Special Controls

Product Code FPK Tubing, Fluid Delivery
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5440
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - FPK Tubing, Fluid Delivery

All 29
Devices cleared under the same product code (FPK) and FDA review panel - the closest regulatory comparables to K950861.
POLYFIN EXTENSION SET, MODELS 126 AND 128
K965208 · Medtronic Minimed · Feb 1997
SILCLEAR TUBING (MODIFICATION)
K953864 · Degania Silicone , Ltd. · Nov 1995
SYSMEX SF-3000
K950508 · Sysmex Corp. · Nov 1995
SILCLEAR TUBING
K943992 · Degania Silicone , Ltd. · Mar 1995
OPHTHALMIC FLUID DISTRIBUTION SETS
K923972 · Visitec Co. · Nov 1992
LO-PROFILE EXTENSION SET
K915560 · Douglas Medical Products Corp. · May 1992