FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FINNIGAN MAT INCOS 50
K Number: K873603
·
Decision Sep 22, 1987
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
21
Applicant Total
4
Review Days
18
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Basic Information
- Device Name
- FINNIGAN MAT INCOS 50
- K Number
- K873603
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.2540
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Finnigan Corp.
- Date Received
- September 4, 1987
- Decision Date
- September 22, 1987
- Product Code
- JJO
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JJO | Flame Emission Photometer For Clinical Use | FDA class 1 | Clinical Chemistry |
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