Cleared Traditional

K983069 - PHILIPS DUO DIAGNOST

K983069 is an FDA 510(k) clearance for PHILIPS DUO DIAGNOST, manufactured by Philips Medical Systems North America, Inc.. The device is a Class 2 Radiology device with product code OWB cleared through the Traditional 510(k) pathway after a 61-day FDA review.

K983069 · Philips Medical Systems North America, Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1998
Decision
61d
Days
Class 2
Risk

K983069 is an FDA 510(k) clearance for the PHILIPS DUO DIAGNOST. Classified as Interventional Fluoroscopic X-ray System (product code OWB), Class II - Special Controls.

Submitted by Philips Medical Systems North America, Inc. (Shelton, US). The FDA issued a Cleared decision on November 2, 1998 after a review of 61 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1650 - the FDA radiology and imaging software 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 Philips Medical Systems North America, Inc. devices

FDA 510(k) Submission Details - K983069

510(k) Number K983069 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 02, 1998
Decision Date November 02, 1998
Days to Decision 61 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 107d · This submission: 61d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

OWB Device Classification - Class 2, Special Controls

Product Code OWB Interventional Fluoroscopic X-ray System
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
Definition Interventional Fluoroscopy
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 Radiology devices follow this clearance model.

Regulatory Peers - OWB Interventional Fluoroscopic X-ray System

All 301
Devices cleared under the same product code (OWB) and FDA review panel - the closest regulatory comparables to K983069.
UROVIEW 2800
K993687 · Ge Dec Medical Systems · Dec 1999
URF DIGITAL - OT
K992660 · Siemens Medical Solutions USA, Inc. · Nov 1999
C-QUEST
K992103 · Wuestec Medical, Inc. · Sep 1999
PHILIPS OMNIDIAGNOST
K982993 · Philips Medical Systems, Inc. · Sep 1998
TREX TILT C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM, TREX TILT-C
K982427 · Trex Medical Corp. · Sep 1998
INTERVENTIONAL MOBILE DIGITAL IMAGING SYSTEM (HEREIN CALLED IMDIS)
K974355 · Ge Dec Medical Systems · Feb 1998