Cleared Traditional

K080655 - CHRYSALIS

K080655 is an FDA 510(k) clearance for CHRYSALIS, manufactured by Meta Imaging Solutions, LLC. The device is a Class 2 Radiology device with product code KPR cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K080655 · Meta Imaging Solutions, LLC · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
May 2008
Decision
63d
Days
Class 2
Risk

K080655 is an FDA 510(k) clearance for the CHRYSALIS. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Meta Imaging Solutions, LLC (Old Lyme, US). The FDA issued a Cleared decision on May 9, 2008 after a review of 63 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.

FDA 510(k) Submission Details - K080655

510(k) Number K080655 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 07, 2008
Decision Date May 09, 2008
Days to Decision 63 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
44d faster than avg
Panel avg: 107d · This submission: 63d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KPR Device Classification - Class 2, Special Controls

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 352
Devices cleared under the same product code (KPR) and FDA review panel - the closest regulatory comparables to K080655.
CARESTREAM DR LONG LENGTH IMAGING SYSTEM FOR DR 7500 SYSTEM
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DR VISION NEO, DR VISION DOU
K080614 · Almana Medical Imaging · Jun 2008
MEDICATECH, MODEL DDR MAK-800, DDT MAK-1000 FS, DDR MAK-1100 FA
K080582 · Medicatech USA · May 2008
DIGITAL RADIOGRAPHY SYSTEM, MODEL QXR-16
K080553 · Vieworks Co., Ltd. · Apr 2008
FUJIFILM UNITY SPEEDSUITE, MODEL CR-IR 371
K073650 · Fujifilm Medical Systems U.S.A, Inc. · Feb 2008
IMIX INSIGHT X-RAY SYSTEMS
K073114 · Imix Adr Finland OY · Jan 2008
K080655 · CHRYSALIS
Download PDF FDA Summary Meta Imaging Solution…