DOUGLAS MEDICAL PRODUCTS, INC. VENTED SPIKE ADAPT

Set, Administration, Intravascular

DOUGLAS MEDICAL PRODUCTS CORP.

The following data is part of a premarket notification filed by Douglas Medical Products Corp. with the FDA for Douglas Medical Products, Inc. Vented Spike Adapt.

Pre-market Notification Details

Device IDK926184
510k NumberK926184
Device Name:DOUGLAS MEDICAL PRODUCTS, INC. VENTED SPIKE ADAPT
ClassificationSet, Administration, Intravascular
Applicant DOUGLAS MEDICAL PRODUCTS CORP. 345 DUNBAR RD. Mundelein,  IL  60060
ContactDouglas Johnson
CorrespondentDouglas Johnson
DOUGLAS MEDICAL PRODUCTS CORP. 345 DUNBAR RD. Mundelein,  IL  60060
Product CodeFPA  
CFR Regulation Number880.5440 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-12-08
Decision Date1993-07-27

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