FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
COBAS(R) CORE IGE TOTAL EIA
K Number: K930890
·
Decision Aug 5, 1993
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
113
Applicant Total
296
Review Days
164
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Basic Information
- Device Name
- COBAS(R) CORE IGE TOTAL EIA
- K Number
- K930890
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5510
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Roche Diagnostic Systems, Inc.
- Date Received
- February 22, 1993
- Decision Date
- August 5, 1993
- 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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| K983555 | ABUSCREEN ONLINE BENZ 200 CALIBRATORS | Dec 15, 1998 | Substantially Equivalent |
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| K983701 | MODIFICATION TO ABUSCREEN ONLINE FOR CANNABINOIDS | Dec 11, 1998 | Substantially Equivalent |
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