FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
POTASSIUM REAGENT SET
K Number: K813608
·
Decision Jan 22, 1982
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
15
Applicant Total
8
Review Days
24
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Basic Information
- Device Name
- POTASSIUM REAGENT SET
- K Number
- K813608
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1600
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Diagnostic Specialties
- Date Received
- December 29, 1981
- Decision Date
- January 22, 1982
- 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 Diagnostic Specialties
| K Number | Device Name | ||
|---|---|---|---|
| K971458 | ENZIP IMMUNOTURBIDIMETRIC MICROALBUMIN ASSAY KIT | Sep 2, 1997 | Substantially Equivalent |
| K941001 | ENZIP IMMUNOTURBIDMETRIC FIBRINOGEN ASSAY KIT | Aug 30, 1994 | Substantially Equivalent |
| K930823 | PROTEIN-BOUND GLUCOSE ASSAYN KIT | Aug 19, 1993 | Substantially Equivalent |
| K922032 | ENZIP URINARY MICROALBUMIN TEST | Jul 30, 1992 | Substantially Equivalent |
| K831180 | PREGNA-CERT, SLIDE PREGNANCY TEST | May 27, 1983 | Substantially Equivalent |
| K823109 | GENERIC PREGNANCY TEST | Nov 10, 1982 | Substantially Equivalent |
| K813412 | GLUCOSE ENZYME-COLOR REAGENT SET | Dec 31, 1981 | Substantially Equivalent |