FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
RUBEOLA IGM ELISA TEST
K Number: K904083
·
Decision Jan 3, 1991
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
10
Applicant Total
57
Review Days
120
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Basic Information
- Device Name
- RUBEOLA IGM ELISA TEST
- K Number
- K904083
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.3520
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Gull Laboratories, Inc.
- Date Received
- September 5, 1990
- Decision Date
- January 3, 1991
- Product Code
- LJB
- 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 |
|---|---|---|---|
| LJB | Enzyme Linked Immunoabsorbent Assay, Rubeola Igg | FDA class 1 | Microbiology |
Similar 510(k) Clearances
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Other Clearances by Gull Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K983541 | HSV 1+2 IGG ELISA TEST | Feb 26, 1999 | Substantially Equivalent |
| K971857 | MUMPS IGG ELISA TESTY | Nov 4, 1997 | Substantially Equivalent |
| K962343 | TOXO IGG ELISA TEST | Mar 24, 1997 | Substantially Equivalent |
| K935730 | EBNA IGG ELISA TEST | Sep 19, 1995 | Substantially Equivalent |
| K940093 | EBV-EA(D) IGG ELISA TEST | Sep 15, 1995 | Substantially Equivalent |
| K941046 | VZV IGG ELISA TEST | Aug 24, 1995 | Substantially Equivalent |
| K941198 | EBV LGG ELISA TEST | Aug 23, 1995 | Substantially Equivalent |
| K932333 | PROTECTORAL ULTRASONIC HANDPIECE PROCESSOR | Aug 15, 1995 | Substantially Equivalent |
| K941624 | RUBELLA IGG ELISA TEST | Aug 4, 1995 | Substantially Equivalent |
| K922758 | HSV-1 IGM ELISA TEST -- MODIFICATION | Oct 5, 1992 | Substantially Equivalent |