DAUM NEUROBIOPSY NEEDLE

Instrument, Biopsy

DAUM CORP.

The following data is part of a premarket notification filed by Daum Corp. with the FDA for Daum Neurobiopsy Needle.

Pre-market Notification Details

Device IDK974631
510k NumberK974631
Device Name:DAUM NEUROBIOPSY NEEDLE
ClassificationInstrument, Biopsy
Applicant DAUM CORP. P.O. BOX 4341 Crofton,  MD  21114
ContactE.j. Smith
CorrespondentE.j. Smith
DAUM CORP. P.O. BOX 4341 Crofton,  MD  21114
Product CodeKNW  
CFR Regulation Number876.1075 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1997-12-12
Decision Date1998-03-09

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