FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SUSCEPTIBILITY DISK, CINOXACIN 100 MCG.
K Number: K792349
·
Decision Mar 12, 1980
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
2
Applicant Total
30
Review Days
114
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Basic Information
- Device Name
- SUSCEPTIBILITY DISK, CINOXACIN 100 MCG.
- K Number
- K792349
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1575
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Pfizer, Inc.
- Date Received
- November 19, 1979
- Decision Date
- March 12, 1980
- Product Code
- JNT
- Advisory Committee
- Clinical Chemistry
- 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 |
|---|---|---|---|
| JNT | Chromatographic, Phospholipids | FDA class 1 | Clinical Chemistry |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (JNT), ordered by most recent decision date.
ZITHROMAX
FDA 510(k)
FDA Class 1
·Clinical Chemistry
PHOSPHOLIPID REAGENT SET
FDA 510(k)
FDA Class 1
·Clinical Chemistry
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