PM-80 PULMOTESTER

Spirometer, Diagnostic

FUTURE IMPEX CORP.

The following data is part of a premarket notification filed by Future Impex Corp. with the FDA for Pm-80 Pulmotester.

Pre-market Notification Details

Device IDK843984
510k NumberK843984
Device Name:PM-80 PULMOTESTER
ClassificationSpirometer, Diagnostic
Applicant FUTURE IMPEX CORP. 2076 DEER PARK AVE. Deerpark,  NY  11729
ContactMorad Davoudzadeh
CorrespondentMorad Davoudzadeh
FUTURE IMPEX CORP. 2076 DEER PARK AVE. Deerpark,  NY  11729
Product CodeBZG  
CFR Regulation Number868.1840 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-10-11
Decision Date1984-10-24

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