Cleared Traditional

K930761 - IMAGE-X 70 INTRAORAL X-RAY SYSTEM

K930761 is an FDA 510(k) clearance for IMAGE-X 70 INTRAORAL X-RAY SYSTEM, manufactured by Afp Imaging Corp.. The device is a Class 2 Radiology device with product code EAP cleared through the Traditional 510(k) pathway after a 102-day FDA review.

K930761 · Afp Imaging Corp. · Radiology device
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May 1993
Decision
102d
Days
Class 2
Risk

K930761 is an FDA 510(k) clearance for the IMAGE-X 70 INTRAORAL X-RAY SYSTEM. Classified as Unit, X-ray, Intraoral (product code EAP), Class II - Special Controls.

Submitted by Afp Imaging Corp. (Elmsford, US). The FDA issued a Cleared decision on May 25, 1993 after a review of 102 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1810 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Afp Imaging Corp. devices

FDA 510(k) Submission Details - K930761

510(k) Number K930761 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 12, 1993
Decision Date May 25, 1993
Days to Decision 102 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
5d faster than avg
Panel avg: 107d · This submission: 102d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EAP Device Classification - Class 2, Special Controls

Product Code EAP Unit, X-ray, Intraoral
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1810
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 - EAP Unit, X-ray, Intraoral

All 13
Devices cleared under the same product code (EAP) and FDA review panel - the closest regulatory comparables to K930761.
ATLANTIS
K953936 · Trophy Radiologie · Dec 1995
TROPHY RADIOLOGIE RVG RADIOVISIOGRAPHY
K950533 · Trophy Radiologie · Jun 1995
TROPHY RADIOLOGIE RVG PORTABLE RADIOVISIOGRAPHY
K950532 · Trophy Radiologie · Apr 1995
PORTARAY
K792535 · Siemens Corp. · Jan 1980
RAFLEX 70
K792437 · Mdt Corp., Inc. · Jan 1980
GE-700 INTRA ORAL X-RAY SYSTEM
K781630 · General Electric Co. · Dec 1978