RYDER CONTACT LENS CASE MODEL 10670

Case, Contact Lens

BRADSTREET CLINICAL RESEARCH ASSOC., INC.

The following data is part of a premarket notification filed by Bradstreet Clinical Research Assoc., Inc. with the FDA for Ryder Contact Lens Case Model 10670.

Pre-market Notification Details

Device IDK951182
510k NumberK951182
Device Name:RYDER CONTACT LENS CASE MODEL 10670
ClassificationCase, Contact Lens
Applicant BRADSTREET CLINICAL RESEARCH ASSOC., INC. 1588 ROUTE 130 NORTH SUITE C-2 North Brunswick,  NJ  08902
ContactPatricia W Bradstreet
CorrespondentPatricia W Bradstreet
BRADSTREET CLINICAL RESEARCH ASSOC., INC. 1588 ROUTE 130 NORTH SUITE C-2 North Brunswick,  NJ  08902
Product CodeLRX  
CFR Regulation Number886.5928 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-03-16
Decision Date1995-05-16

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