Cleared Traditional

K813506 - FARRORS TMJ CASSETTE HOLDER

K813506 is an FDA 510(k) clearance for FARRORS TMJ CASSETTE HOLDER, manufactured by Brell Mar Products, Inc.. The device is a Class 1 General Hospital device with product code KXF cleared through the Traditional 510(k) pathway after a 45-day FDA review.

K813506 · Brell Mar Products, Inc. · General Hospital
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Jan 1982
Decision
45d
Days
Class 1
Risk

K813506 is an FDA 510(k) clearance for the FARRORS TMJ CASSETTE HOLDER. Classified as Applicator, Absorbent Tipped, Non-sterile (product code KXF), Class I - General Controls.

Submitted by Brell Mar Products, Inc. (Mchenry, US). The FDA issued a Cleared decision on January 29, 1982 after a review of 45 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6025 - the FDA general hospital 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 Brell Mar Products, Inc. devices

FDA 510(k) Submission Details - K813506

510(k) Number K813506 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 15, 1981
Decision Date January 29, 1982
Days to Decision 45 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
84d faster than avg
Panel avg: 129d · This submission: 45d
Pathway characteristics
Predicate-based equivalence.

KXF Device Classification - Class 1, General Controls

Product Code KXF Applicator, Absorbent Tipped, Non-sterile
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6025
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 - KXF Applicator, Absorbent Tipped, Non-sterile

All 15
Devices cleared under the same product code (KXF) and FDA review panel - the closest regulatory comparables to K813506.
IQ CHAMBERS
K992553 · Dormer Laboratories, Inc. · Apr 2000
EAR APPLICATOR, CATALOG NO. 2229
K870762 · Treace Medical, Inc. · Mar 1987
COTTON TIPPED APPLICATORS, SINGLE
K843720 · Abco Dealers, Inc. · Oct 1984
SUBCLAVIAN CATHETER INSERTION TRAY
K802580 · American Pharmaseal Div. Ahsc · Nov 1980
EYE APPLICATORS CAT.#980-983
K802016 · Pollak (Intl.), Ltd. · Sep 1980
PREP SET CAT.#908
K802020 · Pollak (Intl.), Ltd. · Sep 1980