FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
IL 35260, IL TEST AMYLASE REAGENT
K Number: K873572
·
Decision Oct 20, 1987
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
30
Applicant Total
321
Review Days
48
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Basic Information
- Device Name
- IL 35260, IL TEST AMYLASE REAGENT
- K Number
- K873572
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1070
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Instrumentation Laboratory CO
- Date Received
- September 2, 1987
- Decision Date
- October 20, 1987
- Product Code
- CIJ
- 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 |
|---|---|---|---|
| CIJ | Saccharogenic, Amylase | FDA class 2 | Clinical Chemistry |
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