CAREVENT BLS, CAREVENT BLS+, CAREVENT ALS, CAREVENT ALS+, AND CAREVENT ATV— 510(k) K991195

Substantially Equivalent

O-Two Systems Intl., Inc.

FDA 510(k) clearance K991195 for CAREVENT BLS, CAREVENT BLS+, CAREVENT ALS, CAREVENT ALS+, AND CAREVENT ATV, Substantially Equivalent on 1999-04-22. Applicant: O-Two Systems Intl., Inc..

Clearance details

Applicant: O-Two Systems Intl., Inc.
Product code: Code BTL
Advisory panel: Anesthesiology
Date received: 1999-04-08
Decision date: 1999-04-22
Decision: Substantially Equivalent
Clearance type: Special
Location: Ontario L5s 1c8, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code BTL

product code BTL

Death: 8
Malfunction: 3,256
Other: 1
Total: 3,265

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.