FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MONO-TEC
K Number: K841863
·
Decision Jun 13, 1984
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
58
Applicant Total
7
Review Days
40
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Basic Information
- Device Name
- MONO-TEC
- K Number
- K841863
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5640
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Applicant
- Medilab Corp.
- Date Received
- May 4, 1984
- Decision Date
- June 13, 1984
- Product Code
- KTN
- 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 |
|---|---|---|---|
| KTN | System, Test, Infectious Mononucleosis | FDA class 2 | Immunology |
Similar 510(k) Clearances
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DRYSPOT INFECTIOUS MONONUCLEOSIS KIT
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CLEARVIEW IM
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Other Clearances by Medilab Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K841862 | IMMU-TEC | Jun 13, 1984 | Substantially Equivalent |
| K840291 | MCS ALBUMIN REAGENT | Mar 30, 1984 | Substantially Equivalent |
| K840290 | MCS TOTAL PROTEIN REAGENT | Mar 30, 1984 | Substantially Equivalent |
| K840289 | LYSE-TEC | Mar 5, 1984 | Substantially Equivalent |
| K832918 | PREGNA-TEC | Nov 3, 1983 | Substantially Equivalent |
| K832527 | PREGNA-TEC | Sep 12, 1983 | Substantially Equivalent |