FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CDL ISOTONIC DILUENT
K Number: K822501
·
Decision Sep 17, 1982
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
37
Applicant Total
14
Review Days
30
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Basic Information
- Device Name
- CDL ISOTONIC DILUENT
- K Number
- K822501
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 864.8200
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- Connecticut Diagnostics, Ltd.
- Date Received
- August 18, 1982
- Decision Date
- September 17, 1982
- Product Code
- GIF
- 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 |
|---|---|---|---|
| GIF | Diluent, Blood Cell | FDA class 1 | Hematology |
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FDA 510(k)
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Other Clearances by Connecticut Diagnostics, Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K905617 | VISI-STAPH | Mar 29, 1991 | Substantially Equivalent |
| K822500 | CDL LYSING REAGENT | Sep 17, 1982 | Substantially Equivalent |
| K822504 | CDL AUTO-LYSING REAGENT | Sep 17, 1982 | Substantially Equivalent |
| K811222 | INORGANIC PHOSPHORUS REAGENTS | May 21, 1981 | Substantially Equivalent |
| K801898 | URIC ACID DIAGNOSTIC REAGENT | Oct 10, 1980 | Substantially Equivalent |
| K801897 | GLUCOSE DIAGNOSTIC REAGENT | Oct 10, 1980 | Substantially Equivalent |
| K792465 | CONNECTICUT DIAGNOSTICS, LTS. DIRECT | Dec 18, 1979 | Substantially Equivalent |
| K792338 | DONNECT. DIAG. TOTAL BILIRUBIN REAGENTS | Dec 6, 1979 | Substantially Equivalent |
| K792362 | BLOOD UREA NITROGEN REAGENT | Dec 6, 1979 | Substantially Equivalent |
| K792339 | CONNECT. DIAG. ALBUMIN DIAGNOSTIC REAGEN | Dec 6, 1979 | Substantially Equivalent |