LIFELOG(TM)— 510(k) K902962

Substantially Equivalent

Modular Instruments, Inc.

FDA 510(k) clearance K902962 for LIFELOG(TM), Substantially Equivalent on 1990-09-04. Applicant: Modular Instruments, Inc..

Clearance details

Applicant: Modular Instruments, Inc.
Product code: Code BSZ
Advisory panel: Anesthesiology
Date received: 1990-07-05
Decision date: 1990-09-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Malvern, PA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code BSZ

product code BSZ

Death: 23
Injury: 298
Malfunction: 32,987
Total: 33,308

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.