Cleared Traditional

K800102 - STANFORD STERILE LAP SPONGES

K800102 is an FDA 510(k) clearance for STANFORD STERILE LAP SPONGES, manufactured by Lukens Corp.. The device is a Class 1 General & Plastic Surgery device with product code GDY cleared through the Traditional 510(k) pathway after a 12-day FDA review.

K800102 · Lukens Corp. · General & Plastic Surgery device
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Jan 1980
Decision
12d
Days
Class 1
Risk

K800102 is an FDA 510(k) clearance for the STANFORD STERILE LAP SPONGES. Classified as Gauze/sponge, Internal, X-ray Detectable (product code GDY), Class I - General Controls.

Submitted by Lukens Corp. (Mchenry, US). The FDA issued a Cleared decision on January 28, 1980 after a review of 12 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4450 - 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 Lukens Corp. devices

FDA 510(k) Submission Details - K800102

510(k) Number K800102 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 16, 1980
Decision Date January 28, 1980
Days to Decision 12 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
103d faster than avg
Panel avg: 115d · This submission: 12d
Pathway characteristics
Predicate-based equivalence.

GDY Device Classification - Class 1, General Controls

Product Code GDY Gauze/sponge, Internal, X-ray Detectable
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4450
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 - GDY Gauze/sponge, Internal, X-ray Detectable

All 58
Devices cleared under the same product code (GDY) and FDA review panel - the closest regulatory comparables to K800102.
GAUZE SPONGES
K803188 · Abco Dealers, Inc. · Jan 1981
OPRATEX ABDOMINAL PAD
K802798 · Secol Co. · Dec 1980
CONTAIN X-RAY DETECTABLE LAP SPONGE
K801768 · The Buckeye Cellulose Corp. · Aug 1980
STERILIZATION PROCESS/X-RAY DETECT. SPG
K792630 · Procter & Gamble Mfg. Co. · Jan 1980
LAP SPONGE
K782107 · Carapace, Inc. · Feb 1979
SOF-WICKLAP PAD
K780718 · Johnson & Johnson Professionals, Inc. · Jun 1978