INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT— 510(k) K896923

Name: FDA 510(k) clearance K896923
Creator: U.S. Food and Drug Administration
Published: 1990-03-12

Substantially Equivalent for Some Indications

Intertech Resources, Inc.

FDA 510(k) clearance K896923 for INTERTECH/INSPIRON (R) MEDICATION NEBULIZER KIT, Substantially Equivalent for Some Indications on 1990-03-12. Applicant: Intertech Resources, Inc.. Device class: 2.

Clearance details

Applicant: Intertech Resources, Inc.
Product code: Code CAF
Device class: Class 2
Regulation: 21 CFR 868.5630
Advisory panel: Anesthesiology
Date received: 1989-12-12
Decision date: 1990-03-12
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Fort Myers, FL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CAF

product code CAF

Death: 22
Injury: 125
Malfunction: 613
Other: 11
Total: 771

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.