Cleared Traditional

K831492 - YESONA PLASTER OF PARIS BANDAGE

K831492 is the FDA 510(k) clearance for YESONA PLASTER OF PARIS BANDAGE by Watson Phillips Y Cia. Sucs., S.A. DE C.V.. It is a Class 1 Physical Medicine device (product code ITG) cleared through the Traditional 510(k) pathway after a 51-day FDA review.

K831492 · Watson Phillips Y Cia. Sucs., S.A. DE C.V. · Physical Medicine device
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Jun 1983
Decision
51d
Days
Class 1
Risk

K831492 is an FDA 510(k) clearance for the YESONA PLASTER OF PARIS BANDAGE. Classified as Bandage, Cast (product code ITG), Class I - General Controls.

Submitted by Watson Phillips Y Cia. Sucs., S.A. DE C.V. (Mchenry, US). The FDA issued a Cleared decision on June 30, 1983 after a review of 51 days - a notably fast clearance cycle.

This device falls under the Physical Medicine FDA review panel, regulated under 21 CFR 890.3025 - 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 Watson Phillips Y Cia. Sucs., S.A. DE C.V. devices

Submission Details

510(k) Number K831492 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 10, 1983
Decision Date June 30, 1983
Days to Decision 51 days
Submission Type Traditional
Review Panel Physical Medicine (PM)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
64d faster than avg
Panel avg: 115d · This submission: 51d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code ITG Bandage, Cast
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 890.3025
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 - ITG Bandage, Cast

All 15
Devices cleared under the same product code (ITG) and FDA review panel - the closest regulatory comparables to K831492.
NON WETTING UNDERCAST PADDING
K833732 · American Medical Disposable, Inc. · Dec 1983
SOFFBAN ORTHOPEDIC PADDING
K832992 · Smith & Nephew, Inc. · Nov 1983
ORTHOPEDIC CASTING TAPE MAXCAST
K832237 · Cutter Laboratories, Inc. · Aug 1983
ULTRACAST WATERLESS SYNTHETIC RESIN CAST
K813052 · Zimmer, Inc. · Feb 1982
CRYSTONA
K811754 · Smith & Nephew, Inc. · Jul 1981
PROCAST
K791831 · Medical Specialties, Inc. · Sep 1979