FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MISSION CONTROLS
K Number: K033063
·
Decision Dec 12, 2003
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
66
Applicant Total
26
Review Days
74
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Basic Information
- Device Name
- MISSION CONTROLS
- K Number
- K033063
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Diamond Diagnostics, Inc.
- Date Received
- September 29, 2003
- Decision Date
- December 12, 2003
- Product Code
- JJS
- 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 |
|---|---|---|---|
| JJS | Controls For Blood-Gases, (Assayed And Unassayed) | FDA class 1 | Clinical Chemistry |
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| K121040 | SMARTLYTE ELECTROLYTE ANALYZER | Aug 30, 2012 | Substantially Equivalent |
| K121140 | PROLYTE ELECTROLYTE ANALYZER | Aug 22, 2012 | Substantially Equivalent |
| K120591 | DIAMOND TOKYO BOEKI ISE MODULE CALIBRATOR 1,2,1-2 | Apr 17, 2012 | Substantially Equivalent |
| K103364 | MISSION CLINICHECK ASSAYED CHEMISTRY CONTROLS, LEVEL 1, LEVEL 2, DUAL LEVEL | May 6, 2011 | Substantially Equivalent |
| K102959 | PROLYTE ELECTROLYTE ANALYZER | Jan 14, 2011 | Substantially Equivalent |
| K093357 | DIAMOND MEDICA ISE MODULE CALIBRANT A MODEL ME-6370D, DIAMOND MEDICA ISE MODULE CALIBRANT B, MODEL ME-5410D | Jun 24, 2010 | Substantially Equivalent |