FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NAPHTHYL PHOSPHATE, ACID PHOSPHATASE
K Number: K863832
·
Decision Dec 16, 1986
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
44
Applicant Total
74
Review Days
77
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Basic Information
- Device Name
- NAPHTHYL PHOSPHATE, ACID PHOSPHATASE
- K Number
- K863832
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1020
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Pointe Scientific, Inc.,
- Date Received
- September 30, 1986
- Decision Date
- December 16, 1986
- Product Code
- JFH
- 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 |
|---|---|---|---|
| JFH | Acid Phosphatase (Prostatic), Tartrate Inhibited | FDA class 2 | Clinical Chemistry |
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|---|---|---|---|
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| K070251 | CARBON DIOXIDE LIQUID STABLE REAGENT | Apr 30, 2007 | Substantially Equivalent |
| K070207 | MULTI-ANALYTE CHEMISTRY CALIBRATOR | Apr 13, 2007 | Substantially Equivalent |
| K070504 | AMMONIA/ALCOHOL CONTROL SET | Apr 11, 2007 | Substantially Equivalent |
| K061377 | APOLIPOPROTEIN A1 AND APOLIPOPROTEIN B REAGENTS AND CALIBRATORS | Mar 28, 2007 | Substantially Equivalent |
| K051646 | ISE DILUENT, 1N KCL, INTERNAL REFERENCE AND ISE STANDARDS LOW AND HIGH | Oct 7, 2005 | Substantially Equivalent |
| K040391 | TOTAL BILIRUBIN REAGENT SET | Jun 2, 2004 | Substantially Equivalent |
| K031539 | HEMOGLOBIN A1C REAGENT SET | Aug 6, 2003 | Substantially Equivalent |
| K023860 | MICROALBUMIN REAGENT SET AND CALIBRATORS | Apr 28, 2003 | Substantially Equivalent |