LAS-R CERULOPLASMIN TEST

Ceruloplasmin, Antigen, Antiserum, Control

HYLAND THERAPEUTIC DIV., TRAVENOL LABORATORIES

The following data is part of a premarket notification filed by Hyland Therapeutic Div., Travenol Laboratories with the FDA for Las-r Ceruloplasmin Test.

Pre-market Notification Details

Device IDK771795
510k NumberK771795
Device Name:LAS-R CERULOPLASMIN TEST
ClassificationCeruloplasmin, Antigen, Antiserum, Control
Applicant HYLAND THERAPEUTIC DIV., TRAVENOL LABORATORIES 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeDDB  
CFR Regulation Number866.5210 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1977-09-23
Decision Date1977-11-14

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