SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER— 510(k) K140559

Substantially Equivalent

Sechrist Industries, Inc.

FDA 510(k) clearance K140559 for SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER, Substantially Equivalent on 2014-05-30. Applicant: Sechrist Industries, Inc..

Clearance details

Applicant: Sechrist Industries, Inc.
Product code: Code CBF
Advisory panel: Anesthesiology
Date received: 2014-03-05
Decision date: 2014-05-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code CBF

product code CBF

Death: 6
Total: 6

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.