FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
KD 0.02 M CALCIUM CHLORIDE SOLUTION
K Number: K883637
·
Decision Oct 31, 1988
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
180
Applicant Total
41
Review Days
67
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Basic Information
- Device Name
- KD 0.02 M CALCIUM CHLORIDE SOLUTION
- K Number
- K883637
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.5425
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- King Diagnostics, Inc.
- Date Received
- August 25, 1988
- Decision Date
- October 31, 1988
- Product Code
- JPA
- Advisory Committee
- Hematology
- Review Advisory Committee
- HE
- 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 |
|---|---|---|---|
| JPA | System, Multipurpose For In Vitro Coagulation Studies | FDA class 2 | Hematology |
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Other Clearances by King Diagnostics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
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| K931834 | KING SODIUM/POTASSIUM STANDARD MODIFIED | Aug 25, 1993 | Substantially Equivalent |
| K931773 | HDL PRECIPITATING REAGENT (DEXTRAN SULFATE) | Aug 16, 1993 | Substantially Equivalent |
| K931326 | KING DIAGNOSTICS CK REAGENT | Jun 15, 1993 | Substantially Equivalent |
| K923129 | KING DIAGNOSTICS GLUCOSE (HK) REAGENT | Nov 2, 1992 | Substantially Equivalent |
| K922969 | KING DIAGNOSTICS UREA NITROGEN REAGENT | Oct 13, 1992 | Substantially Equivalent |
| K922921 | KING DIAGNOSTICS CHLORIDE REAGENT | Oct 5, 1992 | Substantially Equivalent |
| K923927 | KING DIAGNOSTICS MAGNESIUM REAGENT | Sep 30, 1992 | Substantially Equivalent |
| K923091 | KING DIAGNOSTICS GAMMA GT REAGENT | Sep 9, 1992 | Substantially Equivalent |
| K923128 | KING DIAGNOSTICS CHOLESTEROL REAGENT | Sep 9, 1992 | Substantially Equivalent |