Cleared Traditional

K924999 - AUTOPOLE REGULATOR SYSTEM

K924999 is an FDA 510(k) clearance for AUTOPOLE REGULATOR SYSTEM, manufactured by Escalon Trek Medical. The device is a Class 1 Ophthalmic device with product code KYG cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K924999 · Escalon Trek Medical · Ophthalmic device
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Dec 1992
Decision
83d
Days
Class 1
Risk

K924999 is an FDA 510(k) clearance for the AUTOPOLE REGULATOR SYSTEM. Classified as Device, Irrigation, Ocular Surgery (product code KYG), Class I - General Controls.

Submitted by Escalon Trek Medical (Skillmanl, US). The FDA issued a Cleared decision on December 24, 1992 after a review of 83 days - a notably fast clearance cycle.

This device falls under the Ophthalmic FDA review panel, regulated under 21 CFR 886.4360 - the FDA ophthalmic 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 Escalon Trek Medical devices

FDA 510(k) Submission Details - K924999

510(k) Number K924999 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 02, 1992
Decision Date December 24, 1992
Days to Decision 83 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 110d · This submission: 83d
Pathway characteristics
Predicate-based equivalence.

KYG Device Classification - Class 1, General Controls

Product Code KYG Device, Irrigation, Ocular Surgery
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 886.4360
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 - KYG Device, Irrigation, Ocular Surgery

All 23
Devices cleared under the same product code (KYG) and FDA review panel - the closest regulatory comparables to K924999.
I/V POLE
K935226 · Optical Micro Systems, Inc. · Feb 1994
ELECTRIC I/V POLE OR EIVP2
K935003 · Optical Micro Systems, Inc. · Jan 1994
MODIFIED SITE DISPOSABLE DIAPHRAGM CASSETTE
K925921 · Site Microsurgical Systems, Inc. · Dec 1993
MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS
K922996 · Chiron Vision Corp. · Jul 1992
AQUEOUS PARACENTESIS PIPET
K915808 · Visitec Co. · Mar 1992
SITE DIAPHRAGM CASSETTE
K904186 · Site Microsurgical Systems, Inc. · Nov 1990