EQUI-GUARD (ASPIRATOR FILTER)— 510(k) K902089

Name: FDA 510(k) clearance K902089
Creator: U.S. Food and Drug Administration
Published: 1990-07-06

Substantially Equivalent

Equi-Tron Mfg., Inc.

FDA 510(k) clearance K902089 for EQUI-GUARD (ASPIRATOR FILTER), Substantially Equivalent on 1990-07-06. Applicant: Equi-Tron Mfg., Inc.. Device class: 2.

Clearance details

Applicant: Equi-Tron Mfg., Inc.
Product code: Code GCX
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1990-05-09
Decision date: 1990-07-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Niagara Falls, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code GCX

product code GCX

Death: 9
Malfunction: 592
Other: 2
Total: 603

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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