FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ULTRASCAN IGE ASSAY KIT
K Number: K872968
·
Decision Aug 28, 1987
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
3
Review Days
30
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Basic Information
- Device Name
- ULTRASCAN IGE ASSAY KIT
- K Number
- K872968
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5510
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Applicant
- Specialty Medical Industries, Inc.
- Date Received
- July 29, 1987
- Decision Date
- August 28, 1987
- Product Code
- DGC
- Advisory Committee
- Immunology
- 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 |
|---|---|---|---|
| DGC | Ige, Antigen, Antiserum, Control | FDA class 2 | Immunology |
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