FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CALCITONIN RIA KIT
K Number: K872880
·
Decision Aug 13, 1987
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
19
Applicant Total
2
Review Days
23
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Basic Information
- Device Name
- CALCITONIN RIA KIT
- K Number
- K872880
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1140
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Endocrine Associates, Inc.
- Date Received
- July 21, 1987
- Decision Date
- August 13, 1987
- Product Code
- JKR
- 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 |
|---|---|---|---|
| JKR | Radioimmunoassay, Calcitonin | FDA class 2 | Clinical Chemistry |
Similar 510(k) Clearances
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IMMULITE/IMMULITE 1000 CALCITONIN, MODEL LKCL AND IMMULITE 2000 CALCITONIN, MODEL L2KCL
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CALCITONIN
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Other Clearances by Endocrine Associates, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K872879 | DHEA-S RIA KIT | Oct 23, 1987 | Substantially Equivalent |