FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
QCM-SP1(NORMAL CONCENTTRATION) & SP2(ABNORMAL)
K Number: K852418
·
Decision Jul 15, 1985
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
5
Review Days
38
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Basic Information
- Device Name
- QCM-SP1(NORMAL CONCENTTRATION) & SP2(ABNORMAL)
- K Number
- K852418
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Amf Biological and Diagnostics Co.
- Date Received
- June 7, 1985
- Decision Date
- July 15, 1985
- Product Code
- JJY
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- IM
- 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 |
|---|---|---|---|
| JJY | Multi-Analyte Controls, All Kinds (Assayed) | FDA class 1 | Clinical Chemistry |
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Other Clearances by Amf Biological and Diagnostics Co.
| K Number | Device Name | ||
|---|---|---|---|
| K821931 | ZETA-CORT | Jul 22, 1982 | Substantially Equivalent |
| K821553 | ZETAPHASE T3 UPTAKE DIAGNOSTIC KIT | Jun 25, 1982 | Substantially Equivalent |
| K821554 | ZETAPHASE T4 RADIOIMMUNOASSAY DIAG. KIT | Jun 25, 1982 | Substantially Equivalent |
| K812329 | ZETA-SERA D | Sep 1, 1981 | Substantially Equivalent |