VISI-SWAB OPHTALMIC SPONGE

Sponge, Ophthalmic

VISITEC CO.

The following data is part of a premarket notification filed by Visitec Co. with the FDA for Visi-swab Ophtalmic Sponge.

Pre-market Notification Details

Device IDK902750
510k NumberK902750
Device Name:VISI-SWAB OPHTALMIC SPONGE
ClassificationSponge, Ophthalmic
Applicant VISITEC CO. 7575 COMMERCE COURT Sarasota,  FL  34243 -3218
ContactLiaquat Allarakhia
CorrespondentLiaquat Allarakhia
VISITEC CO. 7575 COMMERCE COURT Sarasota,  FL  34243 -3218
Product CodeHOZ  
CFR Regulation Number886.4790 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-06-22
Decision Date1990-07-26

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