EAR KNIVES

Knife, Ear

SHARPOINT, INC.

The following data is part of a premarket notification filed by Sharpoint, Inc. with the FDA for Ear Knives.

Pre-market Notification Details

Device IDK840764
510k NumberK840764
Device Name:EAR KNIVES
ClassificationKnife, Ear
Applicant SHARPOINT, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJYO  
CFR Regulation Number874.4420 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1984-02-23
Decision Date1984-05-21

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