FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
VISI-STAPH
K Number: K905617
·
Decision Mar 29, 1991
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
19
Applicant Total
14
Review Days
105
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Basic Information
- Device Name
- VISI-STAPH
- K Number
- K905617
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.2660
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Connecticut Diagnostics, Ltd.
- Date Received
- December 14, 1990
- Decision Date
- March 29, 1991
- Product Code
- JWX
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- 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 |
|---|---|---|---|
| JWX | Kit, Screening, Staphylococcus Aureus | FDA class 1 | Microbiology |
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Other Clearances by Connecticut Diagnostics, Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K822500 | CDL LYSING REAGENT | Sep 17, 1982 | Substantially Equivalent |
| K822501 | CDL ISOTONIC DILUENT | 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 |