MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS

Device, Irrigation, Ocular Surgery

CHIRON VISION CORP.

The following data is part of a premarket notification filed by Chiron Vision Corp. with the FDA for Modified Site Diaphragm Cassette For Ophthalmics.

Pre-market Notification Details

Device IDK922996
510k NumberK922996
Device Name:MODIFIED SITE DIAPHRAGM CASSETTE FOR OPHTHALMICS
ClassificationDevice, Irrigation, Ocular Surgery
Applicant CHIRON VISION CORP. 135 GIBRALTAR RD. Horsham,  PA  19044
ContactBrunt Miller
CorrespondentBrunt Miller
CHIRON VISION CORP. 135 GIBRALTAR RD. Horsham,  PA  19044
Product CodeKYG  
CFR Regulation Number886.4360 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1992-06-22
Decision Date1992-07-27

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