FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CLINICARD PHOSPHORUS
K Number: K760030
·
Decision Sep 13, 1976
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
116
Review Days
91
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Basic Information
- Device Name
- CLINICARD PHOSPHORUS
- K Number
- K760030
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1580
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Harleco
- Date Received
- June 14, 1976
- Decision Date
- September 13, 1976
- Product Code
- CEO
- 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 |
|---|---|---|---|
| CEO | Phosphomolybdate (Colorimetric), Inorganic Phosphorus | FDA class 1 | Clinical Chemistry |
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WIENER LAB.FOSFATEMIA UV, MODELS 1X100 ML CAT.N 1382321, 4X20 ML CAT.N 1009311
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Other Clearances by Harleco
| K Number | Device Name | ||
|---|---|---|---|
| K820233 | ULTRAZYME PLUS GAMMA GT(65055-65056) | Feb 12, 1982 | Substantially Equivalent |
| K813427 | ULTRACHEM GLUC-DH | Dec 31, 1981 | Substantially Equivalent |
| K813042 | ULTRACHEM GLUC-DH SET, ITEM #65048 | Nov 10, 1981 | Substantially Equivalent |
| K813039 | ULTRACHEM E-CHOL, ITEM #65025 | Nov 10, 1981 | Substantially Equivalent |
| K813043 | ULTRACHEM CREA ITEM #64972 | Nov 10, 1981 | Substantially Equivalent |
| K813040 | ULTRACHEM CA, ITEM #64975 | Nov 10, 1981 | Substantially Equivalent |
| K813044 | ULTRACHEM ALB, ITEM #64970 | Nov 10, 1981 | Substantially Equivalent |
| K813041 | ULTRAZYME-GT, ITEM #64959 & 65032 | Nov 10, 1981 | Substantially Equivalent |
| K813038 | ULTRACHEM TP, ITEM #64974 | Nov 10, 1981 | Substantially Equivalent |
| K812593 | ULTRA ZYME PLUS CK-1 #64978, 65027 & 28 | Oct 2, 1981 | Substantially Equivalent |