ALLERGAN LENS CASE

Case, Contact Lens

ALLERGAN OPTICAL

The following data is part of a premarket notification filed by Allergan Optical with the FDA for Allergan Lens Case.

Pre-market Notification Details

Device IDK884251
510k NumberK884251
Device Name:ALLERGAN LENS CASE
ClassificationCase, Contact Lens
Applicant ALLERGAN OPTICAL 2525 DUPONT DR. P.O. BOX 19534 Irvine,  CA  92623 -9534
ContactTakruri, Phd
CorrespondentTakruri, Phd
ALLERGAN OPTICAL 2525 DUPONT DR. P.O. BOX 19534 Irvine,  CA  92623 -9534
Product CodeLRX  
CFR Regulation Number886.5928 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1988-10-11
Decision Date1988-12-28

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