Cleared Traditional

K890294 - INTER-PAL C-19 AND INTER-PAL C-38

K890294 is an FDA 510(k) clearance for INTER-PAL C-19 AND INTER-PAL C-38, manufactured by Enrad Corp.. The device is a Class 2 Radiology device with product code JAQ cleared through the Traditional 510(k) pathway after a 378-day FDA review.

K890294 · Enrad Corp. · Radiology device
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Feb 1990
Decision
378d
Days
Class 2
Risk

K890294 is an FDA 510(k) clearance for the INTER-PAL C-19 AND INTER-PAL C-38. Classified as System, Applicator, Radionuclide, Remote-controlled (product code JAQ), Class II - Special Controls.

Submitted by Enrad Corp. (Woodland Hills, US). The FDA issued a Cleared decision on February 1, 1990 after a review of 378 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5700 - 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. Elevated predicate reliance profile. 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 Enrad Corp. devices

FDA 510(k) Submission Details - K890294

510(k) Number K890294 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 19, 1989
Decision Date February 01, 1990
Days to Decision 378 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
271d slower than avg
Panel avg: 107d · This submission: 378d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

JAQ Device Classification - Class 2, Special Controls

Product Code JAQ System, Applicator, Radionuclide, Remote-controlled
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5700
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 - JAQ System, Applicator, Radionuclide, Remote-controlled

All 182
Devices cleared under the same product code (JAQ) and FDA review panel - the closest regulatory comparables to K890294.
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