FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GILFORD C3 COMPLEMENT REAGENT
K Number: K853466
·
Decision Sep 16, 1985
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
43
Applicant Total
10
Review Days
28
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Basic Information
- Device Name
- GILFORD C3 COMPLEMENT REAGENT
- K Number
- K853466
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5240
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Applicant
- Gilford
- Date Received
- August 19, 1985
- Decision Date
- September 16, 1985
- Product Code
- CZW
- Advisory Committee
- Immunology
- Review Advisory Committee
- IM
- 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 |
|---|---|---|---|
| CZW | Complement C3, Antigen, Antiserum, Control | FDA class 2 | Immunology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (CZW), ordered by most recent decision date.
SPAPLUS
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Other Clearances by Gilford
| K Number | Device Name | ||
|---|---|---|---|
| K853465 | GILFORD IMMUNOGLOBULIN G REAGENT | Sep 16, 1985 | Substantially Equivalent |
| K853467 | GILFORD IMMUNOGLOBULIN A REAGENT | Sep 16, 1985 | Substantially Equivalent |
| K853468 | GILFORD C4 COMPLEMENT REAGENT | Sep 16, 1985 | Substantially Equivalent |
| K853469 | GILFORD IMMUNOGLOBULIN M REAGENT | Sep 16, 1985 | Substantially Equivalent |
| K851202 | GILFORD TRI-LEVEL ASSAYED IMMUNOLOGY CONTROL | Apr 29, 1985 | Substantially Equivalent |
| K842500 | DATA MGMT. SYSTEM | Aug 16, 1984 | Substantially Equivalent |
| K840120 | ADVANTAGE | Mar 23, 1984 | Substantially Equivalent |
| K833067 | IMPACT 400 #1447X2 | Dec 8, 1983 | Substantially Equivalent |
| K812787 | EIA RUBELLA | Nov 27, 1981 | Substantially Equivalent |