Cleared Traditional

K843587 - PETIT BANDS

K843587 is an FDA 510(k) clearance for PETIT BANDS, manufactured by Micori Gifts, Inc.. The device is a Class 1 General & Plastic Surgery device with product code KGX cleared through the Traditional 510(k) pathway after a 102-day FDA review.

K843587 · Micori Gifts, Inc. · General & Plastic Surgery device
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Nov 1984
Decision
102d
Days
Class 1
Risk

K843587 is an FDA 510(k) clearance for the PETIT BANDS. Classified as Tape And Bandage, Adhesive (product code KGX), Class I - General Controls.

Submitted by Micori Gifts, Inc. (Los Angeles, US). The FDA issued a Cleared decision on November 27, 1984 after a review of 102 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Micori Gifts, Inc. devices

FDA 510(k) Submission Details - K843587

510(k) Number K843587 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 17, 1984
Decision Date November 27, 1984
Days to Decision 102 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
13d faster than avg
Panel avg: 115d · This submission: 102d
Pathway characteristics
Predicate-based equivalence.

KGX Device Classification - Class 1, General Controls

Product Code KGX Tape And Bandage, Adhesive
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 - KGX Tape And Bandage, Adhesive

All 91
Devices cleared under the same product code (KGX) and FDA review panel - the closest regulatory comparables to K843587.
LEUKOPOR SURGICAL TAPE
K843874 · Beiersdorf, Inc. · Feb 1985
LEUKOSILK
K843875 · Beiersdorf, Inc. · Feb 1985
LEUKOFLEX SURGICAL TAPE
K843876 · Beiersdorf, Inc. · Feb 1985
DISPOSABLE LATEX BANDAGE
K842301 · Inmed Corp. · Nov 1984
BAND-AID BRAND ADHESIVE BANDAGE-MEDICA
K842511 · Johnson & Johnson Professionals, Inc. · Nov 1984
MEDICAL TAPE
K840446 · Lectec Corp. · Oct 1984