DeviceClearance

K023793

Substantially Equivalent

1ST RESPONSE INTERMEDIATE MANUAL RESUSCITATOR

Applicant
Portex, Inc.
Product code
BTM
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Keene, NH, US
Download summary PDF View on FDA.gov ↗

Adverse events under product code BTM

product code BTM
Death
19
Other
2
Total
21

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.