TORQUE FRAME QTF1000

System, Isokinetic Testing And Evaluation

MEDMETRIC CORP.

The following data is part of a premarket notification filed by Medmetric Corp. with the FDA for Torque Frame Qtf1000.

Pre-market Notification Details

Device IDK904898
510k NumberK904898
Device Name:TORQUE FRAME QTF1000
ClassificationSystem, Isokinetic Testing And Evaluation
Applicant MEDMETRIC CORP. 7542 TRADE ST. San Diego,  CA  92121 -2412
ContactWatkins
CorrespondentWatkins
MEDMETRIC CORP. 7542 TRADE ST. San Diego,  CA  92121 -2412
Product CodeIKK  
CFR Regulation Number890.1925 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-10-30
Decision Date1990-11-28

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