FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ESTRIOL KIT
K Number: K811380
·
Decision Jun 9, 1981
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
41
Applicant Total
5
Review Days
25
Basic Information
- Device Name
- ESTRIOL KIT
- K Number
- K811380
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1265
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- CAMBRIDGE NUCLEAR CORP.
- Date Received
- May 15, 1981
- Decision Date
- June 9, 1981
- Product Code
- CGI
- 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 |
|---|---|---|---|
| CGI | Radioimmunoassay, Estriol | FDA class 1 | Clinical Chemistry |
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