9000 SERIES FILTER & FILTER/HME— 510(k) K963053

Name: FDA 510(k) clearance K963053
Creator: U.S. Food and Drug Administration
Published: 1997-02-21

Substantially Equivalent

Enternet Medical, Inc.

FDA 510(k) clearance K963053 for 9000 SERIES FILTER & FILTER/HME, Substantially Equivalent on 1997-02-21. Applicant: Enternet Medical, Inc.. Device class: 2.

Clearance details

Applicant: Enternet Medical, Inc.
Product code: Code CAH
Device class: Class 2
Regulation: 21 CFR 868.5260
Advisory panel: Anesthesiology
Date received: 1996-08-06
Decision date: 1997-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Las Vegas, NV, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CAH

product code CAH

Death: 7
Total: 7

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.