FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
G7 AUTOMATED HPLC ANALYZER
K Number: K011434
·
Decision Sep 18, 2001
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
41
Review Days
131
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Basic Information
- Device Name
- G7 AUTOMATED HPLC ANALYZER
- K Number
- K011434
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.7470
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Tosoh Medics, Inc.
- Date Received
- May 10, 2001
- Decision Date
- September 18, 2001
- 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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