AEROSOL MASKS/ADULT & PAEDIATRIC

Mask, Oxygen

DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.

The following data is part of a premarket notification filed by Dhd Medical Products Div. Diemolding Corp. with the FDA for Aerosol Masks/adult & Paediatric.

Pre-market Notification Details

Device IDK860870
510k NumberK860870
Device Name:AEROSOL MASKS/ADULT & PAEDIATRIC
ClassificationMask, Oxygen
Applicant DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP. DIVISION OF DIEMOLDING CORP. Canastota,  NY  13032
ContactRonald N Mchenry
CorrespondentRonald N Mchenry
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP. DIVISION OF DIEMOLDING CORP. Canastota,  NY  13032
Product CodeBYG  
CFR Regulation Number868.5580 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-02-25
Decision Date1986-03-19

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