FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
IGG
K Number: K983221
·
Decision Nov 4, 1998
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
75
Applicant Total
883
Review Days
51
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Basic Information
- Device Name
- IGG
- K Number
- K983221
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5510
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Abbott Laboratories
- Date Received
- September 14, 1998
- Decision Date
- November 4, 1998
- Product Code
- DEW
- 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 |
|---|---|---|---|
| DEW | Igg, Antigen, Antiserum, Control | FDA class 2 | Immunology |
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