Cleared Traditional

K854006 - PLASTELAST AND/OR ELASTOPLASTE

K854006 is the FDA 510(k) clearance for PLASTELAST AND/OR ELASTOPLASTE by Cp Medical. It is a Class 1 General & Plastic Surgery device (product code KGX) cleared through the Traditional 510(k) pathway after a 56-day FDA review.

K854006 · Cp Medical · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1985
Decision
56d
Days
Class 1
Risk

K854006 is an FDA 510(k) clearance for the PLASTELAST AND/OR ELASTOPLASTE. Classified as Tape And Bandage, Adhesive (product code KGX), Class I - General Controls.

Submitted by Cp Medical (Costa Mesa, US). The FDA issued a Cleared decision on November 25, 1985 after a review of 56 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 Cp Medical devices

Submission Details

510(k) Number K854006 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 30, 1985
Decision Date November 25, 1985
Days to Decision 56 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
59d faster than avg
Panel avg: 115d · This submission: 56d
Pathway characteristics
Predicate-based equivalence.

Device Classification

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 73
Devices cleared under the same product code (KGX) and FDA review panel - the closest regulatory comparables to K854006.
LIGHTPLAST(TM)
K872975 · Beiersdorf, Inc. · Aug 1987
THE GRIPPER SEAL(TM)
K870900 · Pharmacia Deltec, Inc. · Mar 1987
LEUKOPLAST(R) POROUS AND SPORT TAPE
K864160 · Beiersdorf, Inc. · Nov 1986
SURGICAL TAPES CLOTH, PAPER & PLASTIC-BASE
K853820 · Abco Dealers, Inc. · Oct 1985
SHEER ADHESIVE BANDAGES, STERILE
K850529 · Abco Dealers, Inc. · May 1985
LEUKOFIX R
K843873 · Beiersdorf, Inc. · Feb 1985