SWIFT LT

Ventilator, Non-continuous (respirator)

RESMED LTD.

The following data is part of a premarket notification filed by Resmed Ltd. with the FDA for Swift Lt.

Pre-market Notification Details

Device IDK073638
510k NumberK073638
Device Name:SWIFT LT
ClassificationVentilator, Non-continuous (respirator)
Applicant RESMED LTD. 14040 DANIELSON ST. Poway,  CA  92064 -6857
ContactDavid D'cruz
CorrespondentDavid D'cruz
RESMED LTD. 14040 DANIELSON ST. Poway,  CA  92064 -6857
Product CodeBZD  
CFR Regulation Number868.5905 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2007-12-26
Decision Date2008-03-20
Summary:summary

Trademark Results [SWIFT LT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SWIFT LT
SWIFT LT
74563358 1923452 Dead/Cancelled
I.Q. Engineering
1994-08-15

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.