BABI PLUS INFANT NASAL CANNULA SYSTEM— 510(k) K110471

Substantially Equivalent

A Plus Medical

FDA 510(k) clearance K110471 for BABI PLUS INFANT NASAL CANNULA SYSTEM, Substantially Equivalent on 2011-10-07. Applicant: A Plus Medical.

Clearance details

Applicant: A Plus Medical
Product code: Code BZD
Advisory panel: Anesthesiology
Date received: 2011-02-18
Decision date: 2011-10-07
Decision: Substantially Equivalent
Clearance type: Special
Location: Carlsbad, CA, US

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Adverse events under product code BZD

product code BZD

Death: 4,440
Injury: 53,099
Malfunction: 213,222
Other: 17
Total: 270,778

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.