FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
KETONE TEST A SANWA STANDARD
K Number: K903367
·
Decision Nov 20, 1990
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
23
Applicant Total
5
Review Days
117
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Basic Information
- Device Name
- KETONE TEST A SANWA STANDARD
- K Number
- K903367
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1435
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Ihara Medics U.S., Inc.
- Date Received
- July 26, 1990
- Decision Date
- November 20, 1990
- Product Code
- JIN
- 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 |
|---|---|---|---|
| JIN | Nitroprusside, Ketones (Urinary, Non-Quant.) | FDA class 1 | Clinical Chemistry |
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