FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DIABETES RISK DETECTOR
K Number: K864544
·
Decision Jul 27, 1987
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
80
Applicant Total
3
Review Days
250
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Basic Information
- Device Name
- DIABETES RISK DETECTOR
- K Number
- K864544
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1340
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Pearce Clinical Laboratories, Inc.
- Date Received
- November 19, 1986
- Decision Date
- July 27, 1987
- Product Code
- JIL
- 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 |
|---|---|---|---|
| JIL | Method, Enzymatic, Glucose (Urinary, Non-Quantitative) | FDA class 2 | Clinical Chemistry |
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