FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CBR-T3 UPTAKE KIT
K Number: K780500
·
Decision May 3, 1978
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
92
Applicant Total
4
Review Days
36
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Basic Information
- Device Name
- CBR-T3 UPTAKE KIT
- K Number
- K780500
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1715
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Clinical Bioresearch
- Date Received
- March 28, 1978
- Decision Date
- May 3, 1978
- Product Code
- KHQ
- 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 |
|---|---|---|---|
| KHQ | Radioassay, Triiodothyronine Uptake | FDA class 2 | Clinical Chemistry |
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