AUTOPOLE REGULATOR SYSTEM— 510(k) K924999

Substantially Equivalent

Escalon Trek Medical

FDA 510(k) clearance K924999 for AUTOPOLE REGULATOR SYSTEM, Substantially Equivalent on 1992-12-24. Applicant: Escalon Trek Medical. Device class: 1.

Clearance details

Applicant: Escalon Trek Medical
Product code: Code KYG
Device class: Class 1
Regulation: 21 CFR 886.4360
Advisory panel: Ophthalmic
Date received: 1992-10-02
Decision date: 1992-12-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skillmanl, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KYG

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K993591 — BLADEWORKS DISPOSABLE ALK TUBING1999-12-28
K981116 — SOVEREIGN CATARACT EXTRACTION SYSTEM1998-05-19
K980647 — EYE IRRIGATOR MODEL #20201998-05-15

More clearances from Escalon Trek Medical

K963417 — VITLITE (TR7700)1996-12-20
K963434 — VISCOUS FLUID SYSTEM1996-11-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.