FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GLYCOHEMOGLOBIN IN WHOLE BLOOD
K Number: K802721
·
Decision Dec 11, 1980
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
231
Review Days
41
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Basic Information
- Device Name
- GLYCOHEMOGLOBIN IN WHOLE BLOOD
- K Number
- K802721
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.7470
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- Sigma Chemical Co.
- Date Received
- October 31, 1980
- Decision Date
- December 11, 1980
- Product Code
- LCP
- Advisory Committee
- Hematology
- Review Advisory Committee
- HE
- 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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