FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
VALIDATE Anemia Calibration Verification/ Linearity Test Kit
K Number: K142964
·
Decision Apr 30, 2015
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
7
Review Days
198
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Basic Information
- Device Name
- VALIDATE Anemia Calibration Verification/ Linearity Test Kit
- K Number
- K142964
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Maine Standards Company, LLC
- Date Received
- October 14, 2014
- Decision Date
- April 30, 2015
- Product Code
- JJY
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JJY | Multi-Analyte Controls, All Kinds (Assayed) | FDA class 1 | Clinical Chemistry |
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Other Clearances by Maine Standards Company, LLC
| K Number | Device Name | ||
|---|---|---|---|
| K170864 | VALIDATE D-Dimer Calibration Verification / Linearity Test Kit | Jun 21, 2017 | Substantially Equivalent |
| K163498 | VALIDATE Heparin Calibration Verification/Linearity Test Kit | Mar 16, 2017 | Substantially Equivalent |
| K162705 | VALIDATE® D-Dimer Calibration Verification/ Linearity Test Kit | Jan 5, 2017 | Substantially Equivalent |
| K152961 | VALIDATE D-Dimer Calibration Verification/Linearity Test Kit | Jun 3, 2016 | Substantially Equivalent |
| K133550 | VALIDATE FERRITIN CALIBRATION VERIFICATION/ LINEARITY TEST KIT | Feb 5, 2014 | Substantially Equivalent |
| K110880 | VALIDATE (R) GC3 CALIBRATION VERIFICATION / LINEARITY TEST KIT | Jul 5, 2011 | Substantially Equivalent |