PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR

Sterilant, Medical Devices

COTTRELL, LTD.

The following data is part of a premarket notification filed by Cottrell, Ltd. with the FDA for Procide 14 N.s., Omnicide/liquid & Plus Liq Activator.

Pre-market Notification Details

Device IDK932922
510k NumberK932922
Device Name:PROCIDE 14 N.S., OMNICIDE/LIQUID & PLUS LIQ ACTIVATOR
ClassificationSterilant, Medical Devices
Applicant COTTRELL, LTD. 7399 SOUTH TUCSON WAY Englewood,  CO  80112
ContactJack Scoville
CorrespondentJack Scoville
COTTRELL, LTD. 7399 SOUTH TUCSON WAY Englewood,  CO  80112
Product CodeMED  
CFR Regulation Number880.6885 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-06-15
Decision Date1995-07-03

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