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510(k) K834467

Device
SPECIMEN TRAP
Applicant
MICROVASIVE
510(k) number
K834467
Product code
BYZ  
Decision
Substantially Equivalent (SESE)
Decision date
1984-02-17
Date received
1983-12-20
Regulation
880.6740
Classification name
Trap, Sterile Specimen
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code BYZ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K925412ELECTROMEDICS TISSUE TRAP/ #TT280Electromedics, Inc.1993-02-05
K913643MUCOUS SPECIMEN TRAPMedical Device Inspection Co., Inc.1991-10-10
K902883TISSUE/POLYP TRAP SYSTEMTriton Technology, Inc.1990-09-12
K841409BUSH NECK W/PLUGWarne Surgical Products, Ltd.1984-04-18
K840253ONE-WAY AIR VALVEDelta Medical Industries1984-04-05
K822556CRITICAL MEASUREMENT UNITBemis Health Care1982-10-18
K822557SPECIMEN ADAPTORBemis Health Care1982-10-18
K791847ASPRI-LUKEMedical Marketing Group1979-10-02

Legacy Summary#

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FDA Review#

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