Cleared Traditional

K924093 - ELECTRIC HI LO TILT TABLE

K924093 is an FDA 510(k) clearance for ELECTRIC HI LO TILT TABLE, manufactured by Midland Mfg. Co.. The device is a Class 1 Physical Medicine device with product code INQ cleared through the Traditional 510(k) pathway after a 183-day FDA review.

K924093 · Midland Mfg. Co. · Physical Medicine device
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Feb 1993
Decision
183d
Days
Class 1
Risk

K924093 is an FDA 510(k) clearance for the ELECTRIC HI LO TILT TABLE. Classified as Table, Powered (product code INQ), Class I - General Controls.

Submitted by Midland Mfg. Co. (Great Neck, US). The FDA issued a Cleared decision on February 12, 1993 after a review of 183 days - an extended review cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3760 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Physical Medicine review framework, consistent with the majority of Class II 510(k) submissions.

View all Midland Mfg. Co. devices

FDA 510(k) Submission Details - K924093

510(k) Number K924093 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 13, 1992
Decision Date February 12, 1993
Days to Decision 183 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
68d slower than avg
Panel avg: 115d · This submission: 183d
Pathway characteristics
Predicate-based equivalence.

INQ Device Classification - Class 1, General Controls

Product Code INQ Table, Powered
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3760
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 - INQ Table, Powered

All 49
Devices cleared under the same product code (INQ) and FDA review panel - the closest regulatory comparables to K924093.
MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE
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K925594 · Tri W-G, Inc. · Feb 1993
MODEL 600 MEDICAL TREATMENT TABLE
K923325 · Tri W-G, Inc. · Jul 1992
MAT TABLE, 8100 SERIES MAT PLATFORM
K920585 · Tri W-G, Inc. · Apr 1992