FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFICATION TO REFLOTRON AMYLASE, CAT. 1200658
K Number: K011145
·
Decision Jun 25, 2001
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
98
Applicant Total
264
Review Days
91
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Basic Information
- Device Name
- MODIFICATION TO REFLOTRON AMYLASE, CAT. 1200658
- K Number
- K011145
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1070
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Roche Diagnostics Corp.
- Date Received
- March 26, 2001
- Decision Date
- June 25, 2001
- Product Code
- JFJ
- 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 |
|---|---|---|---|
| JFJ | Catalytic Methods, Amylase | FDA class 2 | Clinical Chemistry |
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