VENTI-GARD JR.— 510(k) K810896

Name: FDA 510(k) clearance K810896
Creator: U.S. Food and Drug Administration
Published: 1981-04-17

Substantially Equivalent

Con Med Equipment, Inc.

FDA 510(k) clearance K810896 for VENTI-GARD JR., Substantially Equivalent on 1981-04-17. Applicant: Con Med Equipment, Inc.. Device class: 1.

Clearance details

Applicant: Con Med Equipment, Inc.
Product code: Code KGX
Device class: Class 1
Regulation: 21 CFR 880.5240
Advisory panel: General Hospital
Date received: 1981-04-03
Decision date: 1981-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code KGX

product code KGX

Injury: 1,590
Malfunction: 1,357
Other: 3
Total: 2,950

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.