FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE

K Number: K090338 · Decision May 8, 2009
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
12
Applicant Total
6
Review Days
87

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Basic Information

Device Name
ULTRA LOW TOTAL CHLORINE, E-Z CHEK SENSITIVE TOTAL CHLORINE
K Number
K090338
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5665
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Reprocessing Products Corp
Date Received
February 10, 2009
Decision Date
May 8, 2009
Product Code
MSY
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MSY Strip, Test, Reagent, Residuals For Dialysate, Disinfectant

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MSY), ordered by most recent decision date.

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Other Clearances by Reprocessing Products Corp

K Number Device Name
K123805 E-Z CHEK BLOOD LEAK TEST STRIPS
K101750 RPC E-Z CHEK 6.8-8.5 PH TEST STRIPS, MODEL K100-0117 AND E-Z CHEK 0-14 PH TEST STRIPS, MODEL K100-0104
K974426 POTENCY TEST STRIPS, INDICATOR TEST STRIPS
K974064 MICRO X RESIDUAL TEST STRIPS
K950602 PORT CAPS (PROTECTIVE CLOSURES FOE REPROCESSED HEMODIALYZERS