FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
URIC ACID/IRON/MAGNESIUM LINEARITY STANDARDS
K Number: K904099
·
Decision Oct 26, 1990
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
41
Review Days
50
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Basic Information
- Device Name
- URIC ACID/IRON/MAGNESIUM LINEARITY STANDARDS
- K Number
- K904099
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Hichem Diagnostics
- Date Received
- September 6, 1990
- Decision Date
- October 26, 1990
- Product Code
- JJY
- 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 |
|---|---|---|---|
| JJY | Multi-Analyte Controls, All Kinds (Assayed) | FDA class 1 | Clinical Chemistry |
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Other Clearances by Hichem Diagnostics
| K Number | Device Name | ||
|---|---|---|---|
| K981794 | HICHEM CALCIUM REAGENT KIT | Jul 29, 1998 | Substantially Equivalent |
| K963383 | HICHEM ALP/AMP REAGENT KIT | Sep 23, 1996 | Substantially Equivalent |
| K953862 | HICHEM ISEKCI SOLUTION KIT 70010 | Sep 6, 1995 | Substantially Equivalent |
| K953860 | HICHEM ISE DILUENT KIT 70008 | Sep 6, 1995 | Substantially Equivalent |
| K953861 | HICHEM ISE INTDERNAL REFERENCE KIT 70009 | Sep 6, 1995 | Substantially Equivalent |
| K953863 | HICHEM ISE STANDARDS KIT 70011 | Sep 6, 1995 | Substantially Equivalent |
| K951751 | HICHEM AST REAGENT KIT | Aug 2, 1995 | Substantially Equivalent |
| K946192 | HICHEM Y-GT REAGENT KIT | May 2, 1995 | Substantially Equivalent |
| K946022 | HICHEM LDH/L REAGENT KIT | Feb 23, 1995 | Substantially Equivalent |
| K941433 | HI CHEM AQUEOUS GLUCOSE CONTROL, LOW, MED, HIGH | Aug 2, 1994 | Substantially Equivalent |