PEGASUS NASAL CPAP SYSTEM— 510(k) K022192

Name: FDA 510(k) clearance K022192
Creator: U.S. Food and Drug Administration
Published: 2003-01-24

Substantially Equivalent

Sensor Medics Corp.

FDA 510(k) clearance K022192 for PEGASUS NASAL CPAP SYSTEM, Substantially Equivalent on 2003-01-24. Applicant: Sensor Medics Corp.. Device class: 2.

Clearance details

Applicant: Sensor Medics Corp.
Product code: Code BZD
Device class: Class 2
Regulation: 21 CFR 868.5905
Advisory panel: Anesthesiology
Date received: 2002-07-05
Decision date: 2003-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Yorba Linda, CA, US

Download summary PDF View on FDA.gov ↗

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K032516 — HIOX80 AEROSOL ADAPTER2004-03-04
K031745 — INFANT FLOW PLUS INFANT CPAP SYSTEM WITH SIPAP FUNCTION2004-02-13
K031883 — LYRA NASAL MASK2003-08-25
K030943 — MODIFICATION TO HIOX2003-04-22
K020665 — HI-OX2002-07-30

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.