PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT— 510(k) K963956

Substantially Equivalent

Southern Research, Inc.

FDA 510(k) clearance K963956 for PORTABLE LIQUID OXYGEN UNIT AND STATIONARY LIQUID OXYGEN UNIT, Substantially Equivalent on 1996-12-09. Applicant: Southern Research, Inc..

Clearance details

Applicant: Southern Research, Inc.
Product code: Code BYJ
Advisory panel: Anesthesiology
Date received: 1996-10-02
Decision date: 1996-12-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Neck, NY, US

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Adverse events under product code BYJ

product code BYJ

Death: 16
Total: 16

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.