FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AZOG, INC. HCG ONE-STEP URINE HOME PREGNANCY TEST (DIP STICK, CASSETTE AND MIDSTREAM)
K Number: K041748
·
Decision Aug 9, 2004
Classifications
1
FEI Numbers
117
Registration Numbers
117
Same Product Code
225
Applicant Total
3
Review Days
41
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Basic Information
- Device Name
- AZOG, INC. HCG ONE-STEP URINE HOME PREGNANCY TEST (DIP STICK, CASSETTE AND MIDSTREAM)
- K Number
- K041748
- Device Class
- FDA class 2
- Clearance Type
- Abbreviated
- Regulation Number
- 862.1155
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Azog, Inc.
- Date Received
- June 29, 2004
- Decision Date
- August 9, 2004
- Product Code
- LCX
- 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 |
|---|---|---|---|
| LCX | Kit, Test, Pregnancy, Hcg, Over The Counter | FDA class 2 | Clinical Chemistry |
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