Cleared Traditional

K040587 - MINI GAMMA CAMERA, MODEL MGC-500

K040587 is an FDA 510(k) clearance for MINI GAMMA CAMERA, manufactured by Acrorad Co., Ltd.. The device is a Class 1 Radiology device with product code IYX cleared through the Traditional 510(k) pathway after a 70-day FDA review.

K040587 · Acrorad Co., Ltd. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2004
Decision
70d
Days
Class 1
Risk

K040587 is an FDA 510(k) clearance for the MINI GAMMA CAMERA, MODEL MGC-500. Classified as Camera, Scintillation (gamma) (product code IYX), Class I - General Controls.

Submitted by Acrorad Co., Ltd. (Brookeville, US). The FDA issued a Cleared decision on May 14, 2004 after a review of 70 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1100 - 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 Acrorad Co., Ltd. devices

FDA 510(k) Submission Details - K040587

510(k) Number K040587 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 05, 2004
Decision Date May 14, 2004
Days to Decision 70 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
37d faster than avg
Panel avg: 107d · This submission: 70d
Pathway characteristics
Predicate-based equivalence.

IYX Device Classification - Class 1, General Controls

Product Code IYX Camera, Scintillation (gamma)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.1100
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - IYX Camera, Scintillation (gamma)

All 75
Devices cleared under the same product code (IYX) and FDA review panel - the closest regulatory comparables to K040587.
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