Cleared Traditional

K960196 - TRI W-G

K960196 is an FDA 510(k) clearance for TRI W-G, manufactured by Tri W-G, Inc.. The device is a Class 1 Physical Medicine device with product code INQ cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K960196 · Tri W-G, Inc. · Physical Medicine device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1996
Decision
22d
Days
Class 1
Risk

K960196 is an FDA 510(k) clearance for the TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777. Classified as Table, Powered (product code INQ), Class I - General Controls.

Submitted by Tri W-G, Inc. (Valley City, US). The FDA issued a Cleared decision on February 7, 1996 after a review of 22 days - a notably fast clearance 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: 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 Tri W-G, Inc. devices

FDA 510(k) Submission Details - K960196

510(k) Number K960196 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 16, 1996
Decision Date February 07, 1996
Days to Decision 22 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
93d faster than avg
Panel avg: 115d · This submission: 22d
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 20
Devices cleared under the same product code (INQ) and FDA review panel - the closest regulatory comparables to K960196.
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
HI-LO TREATMENT TABLES
K933119 · Tri W-G, Inc. · Oct 1993