Cleared Traditional

K992586 - KONICA LASER IMAGER, DRYPRO MODEL 722

K992586 is an FDA 510(k) clearance for KONICA LASER IMAGER, manufactured by Konica Corp.. The device is a Class 2 Radiology device with product code LMC cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K992586 · Konica Corp. · Radiology device
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Oct 1999
Decision
88d
Days
Class 2
Risk

K992586 is an FDA 510(k) clearance for the KONICA LASER IMAGER, DRYPRO MODEL 722. Classified as Camera, Multi Format, Radiological (product code LMC), Class II - Special Controls.

Submitted by Konica Corp. (Mie-Ken, JP). The FDA issued a Cleared decision on October 29, 1999 after a review of 88 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.2040 - 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 Konica Corp. devices

FDA 510(k) Submission Details - K992586

510(k) Number K992586 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 02, 1999
Decision Date October 29, 1999
Days to Decision 88 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
19d faster than avg
Panel avg: 107d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LMC Device Classification - Class 2, Special Controls

Product Code LMC Camera, Multi Format, Radiological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.2040
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 - LMC Camera, Multi Format, Radiological

All 63
Devices cleared under the same product code (LMC) and FDA review panel - the closest regulatory comparables to K992586.
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