FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HEMOGLOBIN ALC BY COLUMN TEST
K Number: K822977
·
Decision Nov 16, 1982
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
319
Review Days
39
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Basic Information
- Device Name
- HEMOGLOBIN ALC BY COLUMN TEST
- K Number
- K822977
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.7470
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- Bio-Rad
- Date Received
- October 8, 1982
- Decision Date
- November 16, 1982
- 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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