LIFE PAC— 510(k) K854807

Substantially Equivalent

Lifemed Technologies, Inc.

FDA 510(k) clearance K854807 for LIFE PAC, Substantially Equivalent on 1986-04-15. Applicant: Lifemed Technologies, Inc..

Clearance details

Applicant: Lifemed Technologies, Inc.
Product code: Code KZD
Advisory panel: General Hospital
Date received: 1985-12-03
Decision date: 1986-04-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KZD

product code KZD

Death: 4
Total: 4

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.