ESPRIT VENTILATOR NEONATAL OPTION, MODEL V1000— 510(k) K051262

Substantially Equivalent

Respironics California, Inc.

FDA 510(k) clearance K051262 for ESPRIT VENTILATOR NEONATAL OPTION, MODEL V1000, Substantially Equivalent on 2005-07-08. Applicant: Respironics California, Inc..

Clearance details

Applicant: Respironics California, Inc.
Product code: Code CBK
Advisory panel: Anesthesiology
Date received: 2005-05-16
Decision date: 2005-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carlsbad, CA, US

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Adverse events under product code CBK

product code CBK

Death: 736
Injury: 3,628
Malfunction: 98,786
Other: 4
Total: 103,154

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.