JOSTRA HL-20 INTEGRATED PERFUSION SYSTEM— 510(k) K943803

Substantially Equivalent

Janus Biomedical, Inc.

FDA 510(k) clearance K943803 for JOSTRA HL-20 INTEGRATED PERFUSION SYSTEM, Substantially Equivalent on 1996-01-30. Applicant: Janus Biomedical, Inc..

Clearance details

Applicant: Janus Biomedical, Inc.
Product code: Code DTQ
Advisory panel: Cardiovascular
Date received: 1994-08-04
Decision date: 1996-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

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Adverse events under product code DTQ

product code DTQ

Death: 123
Malfunction: 4,822
Other: 1
Total: 4,946

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.