BRITT LENS COMPUTER

System, Imaging, Pulsed Echo, Ultrasonic

BRITT CORP., INC.

The following data is part of a premarket notification filed by Britt Corp., Inc. with the FDA for Britt Lens Computer.

Pre-market Notification Details

Device IDK790694
510k NumberK790694
Device Name:BRITT LENS COMPUTER
ClassificationSystem, Imaging, Pulsed Echo, Ultrasonic
Applicant BRITT CORP., INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeIYO  
CFR Regulation Number892.1560 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1979-04-10
Decision Date1979-08-10

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