STORZ DAISY

Instrument, Vitreous Aspiration And Cutting, Ac-powered

STORZ INSTRUMENT CO.

The following data is part of a premarket notification filed by Storz Instrument Co. with the FDA for Storz Daisy.

Pre-market Notification Details

Device IDK854508
510k NumberK854508
Device Name:STORZ DAISY
ClassificationInstrument, Vitreous Aspiration And Cutting, Ac-powered
Applicant STORZ INSTRUMENT CO. 3365 TREE CT. INDUSTRIAL BLVD. St. Louis,  MO  63122 -6694
ContactDan Regan
CorrespondentDan Regan
STORZ INSTRUMENT CO. 3365 TREE CT. INDUSTRIAL BLVD. St. Louis,  MO  63122 -6694
Product CodeHQE  
CFR Regulation Number886.4150 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1985-11-12
Decision Date1986-02-04

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