Q-CATH RM

Display, Cathode-ray Tube, Medical

QUINTON, INC.

The following data is part of a premarket notification filed by Quinton, Inc. with the FDA for Q-cath Rm.

Pre-market Notification Details

Device IDK883031
510k NumberK883031
Device Name:Q-CATH RM
ClassificationDisplay, Cathode-ray Tube, Medical
Applicant QUINTON, INC. 2121 TERRY AVE. Seatle,  WA  98121
ContactRon R Duck
CorrespondentRon R Duck
QUINTON, INC. 2121 TERRY AVE. Seatle,  WA  98121
Product CodeDXJ  
CFR Regulation Number870.2450 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1988-07-19
Decision Date1988-09-20

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