Cleared Traditional

K963723 - LACERATION TRAY

K963723 is an FDA 510(k) clearance for LACERATION TRAY, manufactured by Grand Medical Products. The device is a Class 1 General & Plastic Surgery device with product code LRP cleared through the Traditional 510(k) pathway after a 72-day FDA review.

K963723 · Grand Medical Products · General & Plastic Surgery device
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Nov 1996
Decision
72d
Days
Class 1
Risk

K963723 is an FDA 510(k) clearance for the LACERATION TRAY. Classified as Tray, Surgical (product code LRP), Class I - General Controls.

Submitted by Grand Medical Products (Schaumburg, US). The FDA issued a Cleared decision on November 27, 1996 after a review of 72 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - the FDA general and plastic surgery 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 Grand Medical Products devices

FDA 510(k) Submission Details - K963723

510(k) Number K963723 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 16, 1996
Decision Date November 27, 1996
Days to Decision 72 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 115d · This submission: 72d
Pathway characteristics
Predicate-based equivalence.

LRP Device Classification - Class 1, General Controls

Product Code LRP Tray, Surgical
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
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 - LRP Tray, Surgical

All 10
Devices cleared under the same product code (LRP) and FDA review panel - the closest regulatory comparables to K963723.
OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK
K951811 · Osteotech, Inc. · May 1995
EYE TRAY
K940239 · Cush Medical Products · Jun 1994
GENERAL SURGERY TRAY
K940444 · Cush Medical Products · Mar 1994
EYE TRAY
K912105 · Medical Device Inspection Co., Inc. · Aug 1991
SITE STERILIZATION TRAYS FOR OPHTHALMIC USE
K883098 · Site Microsurgical Systems, Inc. · Aug 1988
KOI(TM) INSTRUMENT TRAYS
K881095 · CooperVision, Inc. · Apr 1988