Cleared Traditional

K792590 - AP-1 AUTO PROGRAMMER

K792590 is an FDA 510(k) clearance for AP-1 AUTO PROGRAMMER, manufactured by Burdick Corp.. The device is a Class 1 Physical Medicine device with product code IOL cleared through the Traditional 510(k) pathway after a 18-day FDA review.

K792590 · Burdick Corp. · Physical Medicine device
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Jan 1980
Decision
18d
Days
Class 1
Risk

K792590 is an FDA 510(k) clearance for the AP-1 AUTO PROGRAMMER. Classified as Treadmill, Powered (product code IOL), Class I - General Controls.

Submitted by Burdick Corp. (Mchenry, US). The FDA issued a Cleared decision on January 4, 1980 after a review of 18 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.5380 - the FDA physical medicine device 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 Burdick Corp. devices

FDA 510(k) Submission Details - K792590

510(k) Number K792590 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 17, 1979
Decision Date January 04, 1980
Days to Decision 18 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
97d faster than avg
Panel avg: 115d · This submission: 18d
Pathway characteristics
Predicate-based equivalence.

IOL Device Classification - Class 1, General Controls

Product Code IOL Treadmill, Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.5380
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - IOL Treadmill, Powered

All 19
Devices cleared under the same product code (IOL) and FDA review panel - the closest regulatory comparables to K792590.
Q65 MEDICAL TREADMILL
K823003 · Quinton, Inc. · Oct 1982
QUINTON Q55 MEDICAL TREADMILL
K820478 · Quinton, Inc. · Mar 1982
SERIES 1800 EXERCISE TREADMILL
K802836 · Marquette Electronics, Inc. · Dec 1980
CARDIO-EXERCISE TREADMILL 550
K771697 · Quinton, Inc. · Sep 1977
TREADMILL STRESS EXERCISE SYSTEM
K770240 · Burdick Corp. · Feb 1977
POWERED TREADMILL (20/ST)
K761040 · Physio-Control Corp. · Dec 1976