CONPHAR-SCHIOETZ TONOMETER

Tonometer, Manual

CONPHAR, INC.

The following data is part of a premarket notification filed by Conphar, Inc. with the FDA for Conphar-schioetz Tonometer.

Pre-market Notification Details

Device IDK813619
510k NumberK813619
Device Name:CONPHAR-SCHIOETZ TONOMETER
ClassificationTonometer, Manual
Applicant CONPHAR, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeHKY  
CFR Regulation Number886.1930 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-12-29
Decision Date1982-02-24

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