Cleared Traditional

K900879 - SOFT-WEDGE(TM) SYRINGE

K900879 is an FDA 510(k) clearance for SOFT-WEDGE(TM) SYRINGE, manufactured by Baxter Healthcare Corp. The device is a Class 2 Cardiovascular device with product code DYG cleared through the Traditional 510(k) pathway after a 73-day FDA review.

K900879 · Baxter Healthcare Corp · Cardiovascular device
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May 1990
Decision
73d
Days
Class 2
Risk

K900879 is an FDA 510(k) clearance for the SOFT-WEDGE(TM) SYRINGE. Classified as Catheter, Flow Directed (product code DYG), Class II - Special Controls.

Submitted by Baxter Healthcare Corp (Santa Ana, US). The FDA issued a Cleared decision on May 10, 1990 after a review of 73 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.1240 - the FDA cardiovascular device oversight 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 Baxter Healthcare Corp devices

FDA 510(k) Submission Details - K900879

510(k) Number K900879 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 26, 1990
Decision Date May 10, 1990
Days to Decision 73 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
52d faster than avg
Panel avg: 125d · This submission: 73d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DYG Device Classification - Class 2, Special Controls

Product Code DYG Catheter, Flow Directed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.1240
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DYG Catheter, Flow Directed

All 69
Devices cleared under the same product code (DYG) and FDA review panel - the closest regulatory comparables to K900879.
INTHERM TEMPORARY OCCLUSION CATHETER
K901287 · Interventional Therapeutics Corp. · Feb 1991
STEALTH DILATION CATHETER SYSTEM/MODIFICATION
K904287 · Target Therapeutics · Jan 1991
TRI ADAPTER W/ADJUSTABLE HEMOSTASIS VALVES
K901247 · Intec Medical, Inc. · Jul 1990
SWAN-GANZ THERMODILUTION EJECTION FRACTION/VOLUME
K896466 · Baxter Healthcare Corp · Feb 1990
CATHETERS FOR BALLOON OCCLUSION FEMORAL ANGIOGRAPH
K892530 · Arrow Intl., Inc. · Sep 1989
BARD CATH LAB THERMODILUTION CATHETER
K893474 · C.R. Bard, Inc. · Sep 1989