Cleared Traditional

C! (K070589) - FDA 510(k) Clearance

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

K070589 · Transphoton Corporation · Radiology device
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Optimized for regulatory review, auditing and printing
Apr 2007
Decision
54d
Days
Class 2
Risk

K070589 is an FDA 510(k) clearance for the C!. Classified as System, Tomography, Computed, Emission (product code KPS), Class II - Special Controls.

Submitted by Transphoton Corporation (Miami, US). The FDA issued a Cleared decision on April 24, 2007 after a review of 54 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1200 - 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 Transphoton Corporation devices

Submission Details

510(k) Number K070589 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 01, 2007
Decision Date April 24, 2007
Days to Decision 54 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
53d faster than avg
Panel avg: 107d · This submission: 54d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KPS System, Tomography, Computed, Emission
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1200
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 - KPS System, Tomography, Computed, Emission

All 172
Devices cleared under the same product code (KPS) and FDA review panel - the closest regulatory comparables to K070589.
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GE VANTAGE PET NEURO SOFTWARE
K062393 · Ge Healthcare · Sep 2006
FULLCARD ANALYSIS
K061587 · Ge Healthcare · Jun 2006
BIOGRAPH 64 AND BIOGRAPH 40
K060631 · Siemens Medical Solutions USA, Inc. · Mar 2006