510(k) K952595

Device
Haemophilus Test Medium (htm)
Applicant
CLINICAL STANDARDS LABORATORIES, INC.
510(k) number
K952595
Product code
JSO
Decision
Substantially Equivalent (SESE)
Decision date
1996-04-10
Date received
1995-06-06
Regulation
866.1700
Classification name
Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton Agar
Medical specialty
Microbiology
Review panel
Microbiology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
JASON J DEGOES
Address
2011 E. University Dr. Rancho Dominguez CA US 90220 90220

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JSO#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K190553HardyCHROM CREHardy Diagnostics2019-04-29
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K171061MRSASelect IIBio-Rad2017-12-28
K162620Remel Spectra ESBLRemel, Inc.2017-05-01
K160512HardyCHROM ESBLHardy Diagnostics2016-11-15
K162076chromID MRSAbioMerieux, Inc.2016-10-25
K151688chromID MRSAbioMerieux, Inc.2016-03-11
K122187VRESELECT CULTURE MEDIUMBio-Rad2012-11-06
K103684VRESELECT CULTURE MEDIUMBio-Rad2011-10-21
K102922HARDYCHROM MRSAHardy Diagnostics2011-05-04
K100589MRSA SELECT - SKIN AND SOFT TISSUE WOUND SPECIMENSBio-Rad2010-10-29
K092407REMEL SPECTRA MRSARemel, Inc.2010-10-08
K092767BBL CHROMAGAR MRSA IIBecton, Dickinson & CO2010-08-20
K092819REMEL SPECTRA VREThermo Fisher Scientific2010-07-15
K091025CHROMID VRE AGAR, MODEL: REF 43 851bioMerieux, Inc.2010-03-02