Cleared Traditional

K792667 - LEUKOCLIP POROS

K792667 is an FDA 510(k) clearance for LEUKOCLIP POROS, manufactured by Beiersdorf, Inc.. The device is a Class 1 General & Plastic Surgery device with product code FPX cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K792667 · Beiersdorf, Inc. · General & Plastic Surgery device
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Jan 1980
Decision
20d
Days
Class 1
Risk

K792667 is an FDA 510(k) clearance for the LEUKOCLIP POROS. Classified as Strip, Adhesive, Closure, Skin (product code FPX), Class I - General Controls.

Submitted by Beiersdorf, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 16, 1980 after a review of 20 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 880.5240 - 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 Beiersdorf, Inc. devices

FDA 510(k) Submission Details - K792667

510(k) Number K792667 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 27, 1979
Decision Date January 16, 1980
Days to Decision 20 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
95d faster than avg
Panel avg: 115d · This submission: 20d
Pathway characteristics
Predicate-based equivalence.

FPX Device Classification - Class 1, General Controls

Product Code FPX Strip, Adhesive, Closure, Skin
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5240
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 - FPX Strip, Adhesive, Closure, Skin

All 19
Devices cleared under the same product code (FPX) and FDA review panel - the closest regulatory comparables to K792667.
FIXOMULL
K792725 · Beiersdorf, Inc. · Mar 1980
LEUKOFIX POROS
K792726 · Beiersdorf, Inc. · Feb 1980
HYPO-ALLERGENIC PLASTIC TAPE
K792136 · National Patent Development Corp. · Jan 1980
HANSAPOR STERILE
K792360 · Beiersdorf, Inc. · Dec 1979
BAND AID* ADHESIVE BANDAGES
K782003 · Johnson & Johnson Professionals, Inc. · Jan 1979
PAPER TAPE, HYPO ALLERGENIC
K781952 · Johnson & Johnson Professionals, Inc. · Dec 1978