FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RUBELISA (RUBESTAT)
K Number: K950227
·
Decision Aug 15, 1995
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
93
Applicant Total
3
Review Days
217
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Basic Information
- Device Name
- RUBELISA (RUBESTAT)
- K Number
- K950227
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.3510
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Bio-Whittaker, Inc., A Cambrex Co.
- Date Received
- January 10, 1995
- Decision Date
- August 15, 1995
- Product Code
- LFX
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- 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 |
|---|---|---|---|
| LFX | Enzyme Linked Immunoabsorbent Assay, Rubella | FDA class 2 | Microbiology |
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