Cleared Traditional

K933621 - HILO TABLE

K933621 is an FDA 510(k) clearance for HILO TABLE, manufactured by Spinalight, Inc.. The device is a Class 1 Physical Medicine device with product code INQ cleared through the Traditional 510(k) pathway after a 172-day FDA review.

K933621 · Spinalight, Inc. · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 1994
Decision
172d
Days
Class 1
Risk

K933621 is an FDA 510(k) clearance for the HILO TABLE. Classified as Table, Powered (product code INQ), Class I - General Controls.

Submitted by Spinalight, Inc. (Woodstock, US). The FDA issued a Cleared decision on January 7, 1994 after a review of 172 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 Spinalight, Inc. devices

FDA 510(k) Submission Details - K933621

510(k) Number K933621 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 19, 1993
Decision Date January 07, 1994
Days to Decision 172 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
57d slower than avg
Panel avg: 115d · This submission: 172d
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 K933621.
CARDON PHYSICAL THERAPY TABLES R27635
K950364 · Cardon Rehabilitation Products, Inc. · Feb 1995
MODEL 747 AND 747-30 EXAM/TREATMENT TABLE
K941720 · Tri W-G, Inc. · May 1994
TREATMENT TABLE MODIFICATION
K936303 · Tri W-G, Inc. · Mar 1994
POWERMATIC MAT PLATFORM
K933578 · Medical Device Inspection Co., Inc. · Nov 1993
POWER WORK TABLE
K933580 · Medical Device Inspection Co., Inc. · Nov 1993
POWERMATIC TREATMENT TABLE
K933581 · Medical Device Inspection Co., Inc. · Nov 1993