FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CIPRO (TM) DIAGNOSTIC POWDER
K Number: K872081
·
Decision Jun 15, 1987
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
13
Applicant Total
2
Review Days
17
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Basic Information
- Device Name
- CIPRO (TM) DIAGNOSTIC POWDER
- K Number
- K872081
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.1640
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Miles Pharmaceuticals
- Date Received
- May 29, 1987
- Decision Date
- June 15, 1987
- Product Code
- JTT
- 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 |
|---|---|---|---|
| JTT | Susceptibility Test Powders, Antimicrobial | FDA class 2 | Microbiology |
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Other Clearances by Miles Pharmaceuticals
| K Number | Device Name | ||
|---|---|---|---|
| K820578 | MEZLIN DIAGNOSTIC REAGENT | May 12, 1982 | Substantially Equivalent |