Cleared Traditional

K944355 - NIPRO BRANDED DISPOSABLE SYRINGES

K944355 is an FDA 510(k) clearance for NIPRO BRANDED DISPOSABLE SYRINGES, manufactured by Nissho Corp.. The device is a Class 2 General Hospital device with product code FMF cleared through the Traditional 510(k) pathway after a 91-day FDA review.

K944355 · Nissho Corp. · General Hospital
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Dec 1994
Decision
91d
Days
Class 2
Risk

K944355 is an FDA 510(k) clearance for the NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES. Classified as Syringe, Piston (product code FMF), Class II - Special Controls.

Submitted by Nissho Corp. (Miami, US). The FDA issued a Cleared decision on December 7, 1994 after a review of 91 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5860 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Nissho Corp. devices

FDA 510(k) Submission Details - K944355

510(k) Number K944355 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 07, 1994
Decision Date December 07, 1994
Days to Decision 91 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
38d faster than avg
Panel avg: 129d · This submission: 91d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FMF Device Classification - Class 2, Special Controls

Product Code FMF Syringe, Piston
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5860
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 - FMF Syringe, Piston

All 316
Devices cleared under the same product code (FMF) and FDA review panel - the closest regulatory comparables to K944355.
DRUG DISPENSING SPIKE
K946190 · Gelman Sciences, Inc. · Mar 1995
MONOJECT(R) PISTON SYRINGES
K945715 · Sherwood Medical Co. · Mar 1995
DISPOSABLE 1CC SYRINGE WITH LUER LOCK
K945588 · Interventional Therapeutics Corp. · Feb 1995
SYRINGE FILTER DEVICES
K941589 · Gelman Sciences, Inc. · Sep 1994
DRUG RECONSTITUTION FILTER DEVICE
K941020 · Gelman Sciences, Inc. · Aug 1994
IRRIGATION TRAY WITH PISTON SYRINGE
K942221 · Trinity Laboratories, Inc. · Aug 1994