510(k) K960888

Device
CHEK-STIX U.T.I. SELF-TEST
Applicant
Bayer Corp.
510(k) number
K960888
Product code
JMT
Decision
Substantially Equivalent (SESE)
Decision date
1996-07-05
Date received
1996-03-04
Regulation
862.1510
Classification name
Diazo (Colorimetric), Nitrite (Urinary, Non-Quant)
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
1
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
ROSANNE M SAVOL
Address
1884 Miles Ave. Elkhart IN US 46514 46514

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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K875248BIOSCAN URINE DIAGNOSTIC REAGENT STRIPSBioscan Instruments, Inc.1988-02-24
K855238BIOTEL (TM)/UTIAmerican Diagnostic Corp.1986-05-09
K840828KYOTEST 8VKyoto Diagnostics, Inc.1984-05-14