Cleared Traditional

K020070 - JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002

K020070 is an FDA 510(k) clearance for JB-70 INTRAORAL X-RAY SYSTEM, manufactured by Progeny, Inc.. The device is a Class 2 Radiology device with product code EHD cleared through the Traditional 510(k) pathway after a 23-day FDA review.

K020070 · Progeny, Inc. · Radiology device
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Optimized for regulatory review, auditing and printing
Feb 2002
Decision
23d
Days
Class 2
Risk

K020070 is an FDA 510(k) clearance for the JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002. Classified as Unit, X-ray, Extraoral With Timer (product code EHD), Class II - Special Controls.

Submitted by Progeny, Inc. (Buffalo Grove, US). The FDA issued a Cleared decision on February 1, 2002 after a review of 23 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1800 - 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 Progeny, Inc. devices

FDA 510(k) Submission Details - K020070

510(k) Number K020070 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 09, 2002
Decision Date February 01, 2002
Days to Decision 23 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
84d faster than avg
Panel avg: 107d · This submission: 23d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EHD Device Classification - Class 2, Special Controls

Product Code EHD Unit, X-ray, Extraoral With Timer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1800
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 - EHD Unit, X-ray, Extraoral With Timer

All 105
Devices cleared under the same product code (EHD) and FDA review panel - the closest regulatory comparables to K020070.
A/T X-RAY 70
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PROMAX, PANORAMIC X-RAY UNIT WITH CEPHALOSTAT
K011619 · Planmeca Oy · Jun 2001
FOCUS
K001729 · Instrumentarium Corp. · Jul 2000
DIMAX 2
K000771 · Planmeca Oy · May 2000