FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GLUCOMETER ENCORE BLOOD GLUCOSE TEST STRIPS
K Number: K964004
·
Decision Feb 10, 1997
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
144
Applicant Total
96
Review Days
126
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Basic Information
- Device Name
- GLUCOMETER ENCORE BLOOD GLUCOSE TEST STRIPS
- K Number
- K964004
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1345
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Bayer Corp.
- Date Received
- October 7, 1996
- Decision Date
- February 10, 1997
- Product Code
- CFR
- 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 |
|---|---|---|---|
| CFR | Hexokinase, Glucose | FDA class 2 | Clinical Chemistry |
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