LUXOR PORCELAIN

Powder, Porcelain

JENERIC IND.

The following data is part of a premarket notification filed by Jeneric Ind. with the FDA for Luxor Porcelain.

Pre-market Notification Details

Device IDK820057
510k NumberK820057
Device Name:LUXOR PORCELAIN
ClassificationPowder, Porcelain
Applicant JENERIC IND. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeEIH  
CFR Regulation Number872.6660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1982-01-11
Decision Date1982-03-02

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