FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
KODAK SURECELL(TM) HCG-URINE TEST KIT
K Number: K902136
·
Decision Jun 28, 1990
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
374
Applicant Total
238
Review Days
49
Basic Information
- Device Name
- KODAK SURECELL(TM) HCG-URINE TEST KIT
- K Number
- K902136
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1155
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- EASTMAN KODAK COMPANY
- Date Received
- May 10, 1990
- Decision Date
- June 28, 1990
- 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 |
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