Cleared Traditional

K841899 - FIRST RESPONSE EMERG. MEDICAL SYS BONES

K841899 is an FDA 510(k) clearance for FIRST RESPONSE EMERG. MEDICAL SYS BONES, manufactured by Reed Products, Inc.. The device is a Class 1 General & Plastic Surgery device with product code KGX cleared through the Traditional 510(k) pathway after a 77-day FDA review.

K841899 · Reed Products, Inc. · General & Plastic Surgery device
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Jul 1984
Decision
77d
Days
Class 1
Risk

K841899 is an FDA 510(k) clearance for the FIRST RESPONSE EMERG. MEDICAL SYS BONES. Classified as Tape And Bandage, Adhesive (product code KGX), Class I - General Controls.

Submitted by Reed Products, Inc. (Walker, US). The FDA issued a Cleared decision on July 23, 1984 after a review of 77 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 Reed Products, Inc. devices

FDA 510(k) Submission Details - K841899

510(k) Number K841899 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 07, 1984
Decision Date July 23, 1984
Days to Decision 77 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
38d faster than avg
Panel avg: 115d · This submission: 77d
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 K841899.
MEDICAL ADHESIVE FOAM TAPE
K840448 · Lectec Corp. · Oct 1984
SKIN TECH. ISOTEX 86L
K840609 · Lectec Corp. · Oct 1984
MICROPOROUS MED. ADHESIVE TAPE
K840447 · Lectec Corp. · Aug 1984
MELOLITE
K833954 · Smith & Nephew, Inc. · Mar 1984
HYPAFIX DRESSING RETENTION SHEET
K833916 · Smith & Nephew, Inc. · Mar 1984
DRESS, SURGICAL ADHESIVE
K833590 · Lectec Corp. · Jan 1984