Cleared Traditional

ID400 SERIES ARMBOARDS (K950631) - FDA 510(k) Clearance

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K950631 · Image Diagnostics, Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1995
Decision
39d
Days
Class 2
Risk

K950631 is an FDA 510(k) clearance for the ID400 SERIES ARMBOARDS. Classified as System, X-ray, Fluoroscopic, Image-intensified (product code JAA), Class II - Special Controls.

Submitted by Image Diagnostics, Inc. (Sterling, US). The FDA issued a Cleared decision on March 24, 1995 after a review of 39 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 Image Diagnostics, Inc. devices

Submission Details

510(k) Number K950631 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 13, 1995
Decision Date March 24, 1995
Days to Decision 39 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
68d faster than avg
Panel avg: 107d · This submission: 39d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JAA System, X-ray, Fluoroscopic, Image-intensified
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1650
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 - JAA System, X-ray, Fluoroscopic, Image-intensified

All 72
Devices cleared under the same product code (JAA) and FDA review panel - the closest regulatory comparables to K950631.
MAX-1000A/R1
K954590 · Toshiba America Medical Systems, In.C · Nov 1995
FLUOREX DTA-400A
K946081 · Toshiba America Medical Systems, In.C · May 1995
SIRESKOP SX
K951358 · Siemens Medical Solutions USA, Inc. · May 1995
NRF SYSTEM
K944973 · Philips Medical Systems (Cleveland), Inc. · Dec 1994
V-MAX OPTIONS
K943447 · Philips Medical Systems (Cleveland), Inc. · Nov 1994
PRESTIGE REMOTE R & F SYSTEM MODELS H, VH & VHD
K943805 · General Electric Co. · Sep 1994