FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BINAX FSH IRMA TEST KIT, IMMUNORADIOMETRIC ASSAY
K Number: K883305
·
Decision Oct 6, 1988
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
87
Applicant Total
30
Review Days
63
Basic Information
- Device Name
- BINAX FSH IRMA TEST KIT, IMMUNORADIOMETRIC ASSAY
- K Number
- K883305
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1300
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- BINAX, INC.
- Date Received
- August 4, 1988
- Decision Date
- October 6, 1988
- Product Code
- CGJ
- 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 |
|---|---|---|---|
| CGJ | Radioimmunoassay, Follicle-Stimulating Hormone | FDA class 1 | Clinical Chemistry |
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