Cleared Traditional

K984111 - FV-RF

K984111 is the FDA 510(k) clearance for FV-RF by Philips Medical Systems (Cleveland), Inc.. It is a Class 2 Radiology device (product code KPR) cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K984111 · Philips Medical Systems (Cleveland), Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 1998
Decision
24d
Days
Class 2
Risk

K984111 is an FDA 510(k) clearance for the FV-RF. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Philips Medical Systems (Cleveland), Inc. (Cleveland, US). The FDA issued a Cleared decision on December 11, 1998 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - 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 (Cleveland), Inc. devices

Submission Details

510(k) Number K984111 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 17, 1998
Decision Date December 11, 1998
Days to Decision 24 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
83d faster than avg
Panel avg: 107d · This submission: 24d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KPR System, X-ray, Stationary
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1680
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 - KPR System, X-ray, Stationary

All 169
Devices cleared under the same product code (KPR) and FDA review panel - the closest regulatory comparables to K984111.
SILHOUETTE FC
K993090 · Ge Medical Systems, Inc. · Oct 1999
REVOLUTION TX/I DIGITAL RADIOGRAPHIC TABLE SYSTEM
K992066 · GE Medical Systems · Aug 1999
SHIMADZU CEILING TUBE SUPPORT CH-30GH
K990715 · Shimadzu Corp. · Apr 1999
SILHOUETTE VR
K982955 · GE Medical Systems · Nov 1998
DIGITAL RADIOGRAPHIC IMAGING SYSTEM
K982196 · GE Medical Systems · Oct 1998
PHILIPS THORAVISION
K981657 · Philips Medical Systems North America, Inc. · Jun 1998