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 | Device Class | Medical Specialty |
|---|---|---|---|
| MSY | Strip, Test, Reagent, Residuals For Dialysate, Disinfectant | FDA class 2 | Gastroenterology, Urology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (MSY), ordered by most recent decision date.
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E-Z CHECK OZONE TEST STRIPS
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SERIM HISENSE ULTRA 0.1, PART NUMBER 5167
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FDA Class 2
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GLUTARTEST 1 REAGENT STRIP
FDA 510(k)
FDA Class 2
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Other Clearances by Reprocessing Products Corp
| K Number | Device Name | ||
|---|---|---|---|
| K123805 | E-Z CHEK BLOOD LEAK TEST STRIPS | Mar 20, 2013 | Substantially Equivalent |
| 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 | Jan 7, 2011 | Substantially Equivalent |
| K974426 | POTENCY TEST STRIPS, INDICATOR TEST STRIPS | Feb 10, 1999 | Substantially Equivalent |
| K974064 | MICRO X RESIDUAL TEST STRIPS | Dec 7, 1998 | Substantially Equivalent |
| K950602 | PORT CAPS (PROTECTIVE CLOSURES FOE REPROCESSED HEMODIALYZERS | Nov 30, 1995 | Substantially Equivalent |