FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
LEIF CENTRIFUGAL CYTOLOGY BUCKET
K Number: K792032
·
Decision Nov 30, 1979
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
2
Applicant Total
1
Review Days
51
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Basic Information
- Device Name
- LEIF CENTRIFUGAL CYTOLOGY BUCKET
- K Number
- K792032
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 864.3300
- Medical Specialty
- Pathology
- Decision
- Substantially Equivalent
- Applicant
- Robert C. Leif, Ph.D.
- Date Received
- October 10, 1979
- Decision Date
- November 30, 1979
- Product Code
- IFB
- Advisory Committee
- Pathology
- Review Advisory Committee
- PA
- 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 |
|---|---|---|---|
| IFB | Cytocentrifuge | FDA class 1 | Pathology |
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