MODIFIED 225/SIMV VOLUME VENTILATOR— 510(k) K884389

Substantially Equivalent

Monaghan Medical Corp.

FDA 510(k) clearance K884389 for MODIFIED 225/SIMV VOLUME VENTILATOR, Substantially Equivalent on 1990-03-12. Applicant: Monaghan Medical Corp..

Clearance details

Applicant
Monaghan Medical Corp.
Product code
Code CBK
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Plattsburgh, NY, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code CBK

product code CBK
Death
736
Injury
3,628
Malfunction
98,786
Other
4
Total
103,154

Source: openFDA MAUDE database, through . 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.