FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
LIQUIPETTE
K Number: K831079
·
Decision Apr 28, 1983
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
3
Applicant Total
4
Review Days
24
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Basic Information
- Device Name
- LIQUIPETTE
- K Number
- K831079
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 864.6160
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- The Kendall Company Div. of Tyco Healthcare Group
- Date Received
- April 4, 1983
- Decision Date
- April 28, 1983
- Product Code
- GJG
- Advisory Committee
- Hematology
- Review Advisory Committee
- HE
- 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 |
|---|---|---|---|
| GJG | Pipette, Quantitative, Hematology | FDA class 1 | Hematology |
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