PURITAN-BENNETT 840 VENTILATORY SYSTEM WITH BILEVEL OPTION— 510(k) K984535

Substantially Equivalent - Subject to Tracking Reg.

Puritan Bennett Corp.

FDA 510(k) clearance K984535 for PURITAN-BENNETT 840 VENTILATORY SYSTEM WITH BILEVEL OPTION, Substantially Equivalent - Subject to Tracking Reg. on 1998-12-28. Applicant: Puritan Bennett Corp..

Clearance details

Applicant
Puritan Bennett Corp.
Product code
Code CBK
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent - Subject to Tracking Reg.
Clearance type
Special
Location
Carlsbad, CA, 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.