FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DIABETES CARE(TM) TEST PACKAGE FOR THE CLC 330(TM)
K Number: K896582
·
Decision Jun 28, 1990
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
3
Review Days
223
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Basic Information
- Device Name
- DIABETES CARE(TM) TEST PACKAGE FOR THE CLC 330(TM)
- K Number
- K896582
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.7470
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- Primus, Inc.
- Date Received
- November 17, 1989
- Decision Date
- June 28, 1990
- Product Code
- LCP
- Advisory Committee
- Hematology
- 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 |
|---|---|---|---|
| LCP | Assay, Glycosylated Hemoglobin | FDA class 2 | Hematology |
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