PERMLASTIC 2

Material, Impression

KERR CORP.

The following data is part of a premarket notification filed by Kerr Corp. with the FDA for Permlastic 2.

Pre-market Notification Details

Device IDK001655
510k NumberK001655
Device Name:PERMLASTIC 2
ClassificationMaterial, Impression
Applicant KERR CORP. 1717 WEST COLLINS AVE. Orange,  CA  92867
ContactColleen Boswell
CorrespondentColleen Boswell
KERR CORP. 1717 WEST COLLINS AVE. Orange,  CA  92867
Product CodeELW  
CFR Regulation Number872.3660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2000-05-31
Decision Date2000-08-10

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