FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BAYER DIAGNOSTICS CLINITEST PREGNANCY TEST
K Number: K023944
·
Decision Feb 11, 2003
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
96
Review Days
77
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Basic Information
- Device Name
- BAYER DIAGNOSTICS CLINITEST PREGNANCY TEST
- K Number
- K023944
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 862.1155
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Bayer Corp.
- Date Received
- November 26, 2002
- Decision Date
- February 11, 2003
- Product Code
- JHI
- 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 |
|---|---|---|---|
| JHI | Visual, Pregnancy Hcg, Prescription Use | FDA class 2 | Clinical Chemistry |
Similar 510(k) Clearances
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