FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AUTOMIX COMPOUNDER Y - ADAPTOR SET
K Number: K890205
·
Decision Oct 27, 1989
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
3
Review Days
282
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Basic Information
- Device Name
- AUTOMIX COMPOUNDER Y - ADAPTOR SET
- K Number
- K890205
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Stedim, Inc.
- Date Received
- January 18, 1989
- Decision Date
- October 27, 1989
- Product Code
- LHI
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| LHI | Set, I.V. Fluid Transfer | FDA class 2 | General Hospital |
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