FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ECHOCLONAL HTSH IRMA
K Number: K860288
·
Decision Apr 11, 1986
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
319
Review Days
73
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Basic Information
- Device Name
- ECHOCLONAL HTSH IRMA
- K Number
- K860288
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1690
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Bio-Rad
- Date Received
- January 28, 1986
- Decision Date
- April 11, 1986
- Product Code
- JLW
- 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 |
|---|---|---|---|
| JLW | Radioimmunoassay, Thyroid-Stimulating Hormone | FDA class 2 | Clinical Chemistry |
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