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510(k) K922858

Device
Multidraw System
Applicant
CAMBRIDGE MULTI-DRAW, INC.
510(k) number
K922858
Product code
GIM
Decision
Unknown (SESK)
Decision date
1992-11-16
Date received
1992-06-15
Regulation
862.1675
Classification name
Tubes, Vacuum Sample, With Anticoagulant
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
STEPHEN WEBSTER
Address
56 Creighton St. Cambridge MA US 02140 02140

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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510(k), Device, Applicant table
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K971221GREINER VACUETTE BLOOD COLLECTION TUBEGreiner America, Inc.1997-05-02
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K945458VACUTAINER BRAND SAFETY-GARD PHLEBOTOMY SYSTEMBd Becton Dickinson Vacutainer Systems Preanalytic1995-02-06
K944814CORVAC PLASTIC BLOOD COLLECTION TUBESherwood Medical Co.1994-12-19
K940058MONOJECT BLOOD COLLECTION TUBES W/SAFETY STOPPERSherwood Medical Co.1994-05-02
K933939BACT/ALERT BLOOD COLLECTION ADAPTER CAP AND INSERTOrganon Teknika Corp.1994-02-07
K933386VACUTAINER BRAND SAFETY-GARD NEEDLE HOLDER & NEEDLE DISPOSABLE CONTAINER SYSTEMBd Becton Dickinson Vacutainer Systems Preanalytic1993-10-12
K922468ANGEL WING SETS -- MODIFIEDMbo Laboratories, Inc.1992-07-10