FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
POTASSIUM REAGENT SET
K Number: K902574
·
Decision Jul 10, 1990
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
15
Applicant Total
36
Review Days
29
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Basic Information
- Device Name
- POTASSIUM REAGENT SET
- K Number
- K902574
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1600
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Tech-Co, Inc.
- Date Received
- June 11, 1990
- Decision Date
- July 10, 1990
- Product Code
- CEJ
- 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 |
|---|---|---|---|
| CEJ | Tetraphenyl Borate, Colorimetry, Potassium | FDA class 2 | Clinical Chemistry |
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Other Clearances by Tech-Co, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K921968 | IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST | Jun 28, 1996 | Substantially Equivalent |
| K923376 | VISUAL HCG PREGNANCY TEST | Oct 1, 1992 | Substantially Equivalent |
| K920766 | T4 EIA BEAD ASSAY | Apr 17, 1992 | Substantially Equivalent |
| K920716 | DIRECT PREGNANCY TEST | Mar 24, 1992 | Substantially Equivalent |
| K901561 | IRON/TOTAL IRON BINDING CAPACITY | May 17, 1990 | Substantially Equivalent |
| K883387 | ALANINE AMINO TRANSFERASE (COLORIMETRIC METHOD) | Oct 13, 1988 | Substantially Equivalent |
| K883683 | HEMOGLOBIN | Oct 6, 1988 | Substantially Equivalent |
| K883386 | CHLORIDE | Oct 6, 1988 | Substantially Equivalent |
| K881172 | BILIRUBIN (DIRECT) | Jun 7, 1988 | Substantially Equivalent |
| K881173 | ASPARTATE AMINOTRANSFERASE (COLORIMETRIC METHOD) | Jun 7, 1988 | Substantially Equivalent |