510(k) K760156

Device
TEST, (IVDP) SMOOTHMUSCLE ANTIBODY
Applicant
ZEUS SCIENTIFIC, INC.
510(k) number
K760156
Product code
DBE  
Decision
Substantially Equivalent (SESE)
Decision date
1976-07-20
Date received
1976-07-02
Regulation
866.5120
Classification name
Antismooth Muscle Antibody, Indirect Immunofluorescent, Antigen, Control
Medical specialty
Immunology
Review panel
Immunology
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 DBE  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K810983ANTISMOOTH MUSCLE ANTIBODY TEST SYSImmuno-Products Industries1981-05-01
K800820AFT TM SYSTEM ANTISMOOTH MUSCLE ANTIBODYCalbiochem-Behring Corp.1980-04-24
K800228IMMUNOP. ANTISMOOTH MUSCLE ANTIBODY KITClinical Sciences, Inc.1980-02-21
K790430MEDICA II-F-ASMA TEST KITMedica Corp.1979-04-23
K771155ANTI-MITOCHONDRIALMeloy Laboratories, Inc.1977-08-04

Legacy Summary#

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FDA Review#

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