LSI6000 THERMAL THERAPY SYSTEM

Pack, Hot Or Cold, Water Circulating

BURKE NEUTECH, INC.

The following data is part of a premarket notification filed by Burke Neutech, Inc. with the FDA for Lsi6000 Thermal Therapy System.

Pre-market Notification Details

Device IDK926151
510k NumberK926151
Device Name:LSI6000 THERMAL THERAPY SYSTEM
ClassificationPack, Hot Or Cold, Water Circulating
Applicant BURKE NEUTECH, INC. 11701 S. BELCHER RD. SUITE 119 Largo,  FL  34643 -5117
ContactRobert E Burke
CorrespondentRobert E Burke
BURKE NEUTECH, INC. 11701 S. BELCHER RD. SUITE 119 Largo,  FL  34643 -5117
Product CodeILO  
CFR Regulation Number890.5720 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-12-07
Decision Date1993-05-26

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