GREINER MINICOLLECT SERUM GEL BLOOD COLLECTION TUBE

Tubes, Vials, Systems, Serum Separators, Blood Collection

GREINER MEDITECH, INC.

The following data is part of a premarket notification filed by Greiner Meditech, Inc. with the FDA for Greiner Minicollect Serum Gel Blood Collection Tube.

Pre-market Notification Details

Device IDK982998
510k NumberK982998
Device Name:GREINER MINICOLLECT SERUM GEL BLOOD COLLECTION TUBE
ClassificationTubes, Vials, Systems, Serum Separators, Blood Collection
Applicant GREINER MEDITECH, INC. 260 GATEWAY DRIVE, SUITE 17A Bel Air,  MD  21014
ContactDoug Harris
CorrespondentDoug Harris
GREINER MEDITECH, INC. 260 GATEWAY DRIVE, SUITE 17A Bel Air,  MD  21014
Product CodeJKA  
CFR Regulation Number862.1675 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1998-08-27
Decision Date1998-10-21
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
39120017578537 K982998 000
39120017578513 K982998 000
39120017570883 K982998 000
39120017570760 K982998 000

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