PLATELIA TOXO IGG KIT

Test, Leukocyte Typing

KALLESTAD DIAG, A DIV. OF ERBAMONT, INC.

The following data is part of a premarket notification filed by Kallestad Diag, A Div. Of Erbamont, Inc. with the FDA for Platelia Toxo Igg Kit.

Pre-market Notification Details

Device IDK894947
510k NumberK894947
Device Name:PLATELIA TOXO IGG KIT
ClassificationTest, Leukocyte Typing
Applicant KALLESTAD DIAG, A DIV. OF ERBAMONT, INC. 2000 LAKE HAZELTINE DR. Chaska,  MN  55318
ContactSusan Tesmer
CorrespondentSusan Tesmer
KALLESTAD DIAG, A DIV. OF ERBAMONT, INC. 2000 LAKE HAZELTINE DR. Chaska,  MN  55318
Product CodeLGO  
CFR Regulation Number864.7675 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1989-08-03
Decision Date1990-03-23

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