DHD METERED DOSE INHALER (MDI) SPACER— 510(k) K913326

Substantially Equivalent

Dhd Diemolding Healthcare Div.

FDA 510(k) clearance K913326 for DHD METERED DOSE INHALER (MDI) SPACER, Substantially Equivalent on 1992-01-07. Applicant: Dhd Diemolding Healthcare Div..

Clearance details

Applicant: Dhd Diemolding Healthcare Div.
Product code: Code CAF
Advisory panel: Anesthesiology
Date received: 1991-07-25
Decision date: 1992-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Canastota, NY, US

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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.