PALPATION PROBE

Forceps, General & Plastic Surgery

NORTHGATE TECHNOLOGIES, INC.

The following data is part of a premarket notification filed by Northgate Technologies, Inc. with the FDA for Palpation Probe.

Pre-market Notification Details

Device IDK911159
510k NumberK911159
Device Name:PALPATION PROBE
ClassificationForceps, General & Plastic Surgery
Applicant NORTHGATE TECHNOLOGIES, INC. 3930 VENTURA DR. Arlington Heights,  IL  60004
ContactSamuella D Emrich
CorrespondentSamuella D Emrich
NORTHGATE TECHNOLOGIES, INC. 3930 VENTURA DR. Arlington Heights,  IL  60004
Product CodeGEN  
CFR Regulation Number878.4800 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1991-03-15
Decision Date1991-03-29

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