CANNULAS

Cannula, Ophthalmic

VISITEC CO.

The following data is part of a premarket notification filed by Visitec Co. with the FDA for Cannulas.

Pre-market Notification Details

Device IDK790243
510k NumberK790243
Device Name:CANNULAS
ClassificationCannula, Ophthalmic
Applicant VISITEC CO. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeHMX  
CFR Regulation Number886.4350 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1978-12-29
Decision Date1979-02-12

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