Cleared Traditional

K873469 - TODD MEDICAL/SKILLED CARE PRODUCTS

K873469 is an FDA 510(k) clearance for TODD MEDICAL/SKILLED CARE PRODUCTS, manufactured by Todd Medical, Inc.. The device is a Class 1 General & Plastic Surgery device with product code LRP cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K873469 · Todd Medical, Inc. · General & Plastic Surgery device
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Oct 1987
Decision
62d
Days
Class 1
Risk

K873469 is an FDA 510(k) clearance for the TODD MEDICAL/SKILLED CARE PRODUCTS. Classified as Tray, Surgical (product code LRP), Class I - General Controls.

Submitted by Todd Medical, Inc. (Brown Deer, US). The FDA issued a Cleared decision on October 29, 1987 after a review of 62 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 Todd Medical, Inc. devices

FDA 510(k) Submission Details - K873469

510(k) Number K873469 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 28, 1987
Decision Date October 29, 1987
Days to Decision 62 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 115d · This submission: 62d
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 11
Devices cleared under the same product code (LRP) and FDA review panel - the closest regulatory comparables to K873469.
SITE STERILIZATION TRAYS FOR OPHTHALMIC USE
K883098 · Site Microsurgical Systems, Inc. · Aug 1988
KOI(TM) INSTRUMENT TRAYS
K881095 · CooperVision, Inc. · Apr 1988
SECURLINE FINE NEEDLE ASPIRATION BIOPSY TRAY
K874665 · Precision Dynamics Corp. · Jan 1988
LACERATION AND INSTRUMENT TRAYS
K873290 · Advantage Medical Systems, Inc. · Sep 1987
LACERATION TRAY
K873439 · Ulti-Med Intl., Inc. · Sep 1987
MASTER KIT B
K861142 · Pro-Lab, Inc. · Jul 1986