Cleared Traditional

K972900 - ULTRASAFE MODEL T200 INJECTOR

K972900 is an FDA 510(k) clearance for ULTRASAFE MODEL T200 INJECTOR, manufactured by Safety Syringes, Inc.. The device is a Class 2 General Hospital device with product code FMF cleared through the Traditional 510(k) pathway after a 204-day FDA review.

K972900 · Safety Syringes, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1998
Decision
204d
Days
Class 2
Risk

K972900 is an FDA 510(k) clearance for the ULTRASAFE MODEL T200 INJECTOR. Classified as Syringe, Piston (product code FMF), Class II - Special Controls.

Submitted by Safety Syringes, Inc. (Arcadia, US). The FDA issued a Cleared decision on February 26, 1998 after a review of 204 days - an extended review cycle.

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 Safety Syringes, Inc. devices

FDA 510(k) Submission Details - K972900

510(k) Number K972900 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 06, 1997
Decision Date February 26, 1998
Days to Decision 204 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
75d slower than avg
Panel avg: 129d · This submission: 204d
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 416
Devices cleared under the same product code (FMF) and FDA review panel - the closest regulatory comparables to K972900.
B-D E ML PEN
K980755 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Apr 1998
TERUMO ALLERGY SYRINGE
K980796 · Terumo Corp. · Apr 1998
ULTRASAFE INJECTION SYSTEM MODEL C200 INJECTOR WITH NEEDLE GUARD
K972877 · Safety Syringes, Inc. · Feb 1998
DAXOR MAX100 SYRINGE (MAX100)
K970419 · Daxor Corporation · Dec 1997
DUPLOJECT (0.5/1.0 ML, 2.0 ML, 5.0 ML)
K973510 · Immuno-U.S., Inc. · Dec 1997
ULTRASAFE INJECTION SYSTEM NEEDLE GUARD, MODELS B50,B100L,B150,B225, AND B300
K972878 · Safety Syringes, Inc. · Oct 1997