FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER
K Number: K000926
·
Decision May 15, 2000
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
37
Applicant Total
47
Review Days
54
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Basic Information
- Device Name
- EASYELECTROLYTE ANALYZER AND RAPIDLYTE ANALYZER
- K Number
- K000926
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1170
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Medica Corp.
- Date Received
- March 22, 2000
- Decision Date
- May 15, 2000
- Product Code
- CGZ
- 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 |
|---|---|---|---|
| CGZ | Electrode, Ion-Specific, Chloride | FDA class 2 | Clinical Chemistry |
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