LH RIA

Radioimmunoassay, Luteinizing Hormone

SYNCOR INTL. CORP.

The following data is part of a premarket notification filed by Syncor Intl. Corp. with the FDA for Lh Ria.

Pre-market Notification Details

Device IDK833854
510k NumberK833854
Device Name:LH RIA
ClassificationRadioimmunoassay, Luteinizing Hormone
Applicant SYNCOR INTL. CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeCEP  
CFR Regulation Number862.1485 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-11-04
Decision Date1984-01-13

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