Cleared Traditional

K875106 - PB-A LEAD-ACID BATTERY CONVERSION KIT (FDA 510(k) Clearance)

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

K875106 · Diagnostic Imaging Specialists Corp. · Radiology device
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Feb 1988
Decision
70d
Days
Class 2
Risk

K875106 is an FDA 510(k) clearance for the PB-A LEAD-ACID BATTERY CONVERSION KIT. Classified as System, X-ray, Mobile (product code IZL), Class II - Special Controls.

Submitted by Diagnostic Imaging Specialists Corp. (St. Malo, Manitoba, CA). The FDA issued a Cleared decision on February 22, 1988 after a review of 70 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1720 - 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 Diagnostic Imaging Specialists Corp. devices

Submission Details

510(k) Number K875106 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 14, 1987
Decision Date February 22, 1988
Days to Decision 70 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
37d faster than avg
Panel avg: 107d · This submission: 70d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code IZL System, X-ray, Mobile
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1720
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 - IZL System, X-ray, Mobile

All 233
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