FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
URIC ACID REAGENT SET
K Number: K914158
·
Decision Feb 21, 1992
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
117
Applicant Total
13
Review Days
157
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Basic Information
- Device Name
- URIC ACID REAGENT SET
- K Number
- K914158
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1775
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Tech Intl. Co.
- Date Received
- September 17, 1991
- Decision Date
- February 21, 1992
- Product Code
- KNK
- 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 |
|---|---|---|---|
| KNK | Acid, Uric, Uricase (Colorimetric) | FDA class 1 | Clinical Chemistry |
Similar 510(k) Clearances
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WIENER LAB URICOSTAT ENZIMATICO AA LIQUIDA
FDA 510(k)
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Other Clearances by Tech Intl. Co.
| K Number | Device Name | ||
|---|---|---|---|
| K915704 | AMYLASE (KINETIC) REAGENT SET | Jun 28, 1996 | Substantially Equivalent |
| K915705 | ACID PHOSPHATASE REAGENT SET | Feb 27, 1992 | Substantially Equivalent |
| K915707 | AMMONIA REAGENT SET | Feb 26, 1992 | Substantially Equivalent |
| K915706 | LIPASE REAGENT SET | Feb 18, 1992 | Substantially Equivalent |
| K915710 | AMYLASE (COLORIMETRIC) REAGENT SET | Jan 30, 1992 | Substantially Equivalent |
| K914160 | CHOLESTEROL REGEANT SET | Jan 30, 1992 | Substantially Equivalent |
| K915709 | CREATINE KINASE-MB (CK-MB) REAGENT SET | Jan 27, 1992 | Substantially Equivalent |
| K914159 | GLUCOSE REAGENT SET | Jan 27, 1992 | Substantially Equivalent |
| K915708 | INORGANIC PHOSPHORUS(COLORIMETRIC) REAGENT SET | Jan 22, 1992 | Substantially Equivalent |
| K914171 | IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE | Dec 18, 1991 | Substantially Equivalent |