MSAS PROFESSIONAL

Device, Galvanic Skin Response Measurement

BIOMERIDIAN, INT.

The following data is part of a premarket notification filed by Biomeridian, Int. with the FDA for Msas Professional.

Pre-market Notification Details

Device IDK993824
510k NumberK993824
Device Name:MSAS PROFESSIONAL
ClassificationDevice, Galvanic Skin Response Measurement
Applicant BIOMERIDIAN, INT. 12411 SOUTH 265 WEST, SUITE F Draper,  UT  84020 -8671
ContactJoe Galloway
CorrespondentJoe Galloway
BIOMERIDIAN, INT. 12411 SOUTH 265 WEST, SUITE F Draper,  UT  84020 -8671
Product CodeGZO  
CFR Regulation Number882.1540 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received1999-11-12
Decision Date2000-01-20
Summary:summary

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