FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
FOLATE 125I RADIOIMMUNOASSAY
K Number: K803060
·
Decision Dec 22, 1980
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
63
Applicant Total
111
Review Days
101
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Basic Information
- Device Name
- FOLATE 125I RADIOIMMUNOASSAY
- K Number
- K803060
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1295
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Corning Medical & Scientific
- Date Received
- September 12, 1980
- Decision Date
- December 22, 1980
- Product Code
- CGN
- 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 |
|---|---|---|---|
| CGN | Acid, Folic, Radioimmunoassay | FDA class 2 | Clinical Chemistry |
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