Q50 MEDICAL TREADMILL

Treadmill, Powered

QUINTON, INC.

The following data is part of a premarket notification filed by Quinton, Inc. with the FDA for Q50 Medical Treadmill.

Pre-market Notification Details

Device IDK862741
510k NumberK862741
Device Name:Q50 MEDICAL TREADMILL
ClassificationTreadmill, Powered
Applicant QUINTON, INC. 2121 TERRY AVE. Seatle,  WA  98121
ContactRandy Walls
CorrespondentRandy Walls
QUINTON, INC. 2121 TERRY AVE. Seatle,  WA  98121
Product CodeIOL  
CFR Regulation Number890.5380 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1986-07-21
Decision Date1986-07-29

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