FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TRI-TUBE RIA
K Number: K840589
·
Decision Mar 9, 1984
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
92
Applicant Total
24
Review Days
29
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Basic Information
- Device Name
- TRI-TUBE RIA
- K Number
- K840589
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1715
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Nuclear Medical Laboratories, Inc.
- Date Received
- February 9, 1984
- Decision Date
- March 9, 1984
- Product Code
- KHQ
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| KHQ | Radioassay, Triiodothyronine Uptake | FDA class 2 | Clinical Chemistry |
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Other Clearances by Nuclear Medical Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K852438 | NML TSH IRMA | Jul 12, 1985 | Substantially Equivalent |
| K844583 | TSH-STAT | Mar 5, 1985 | Substantially Equivalent |
| K840466 | NML CORTISOL RIA | Mar 30, 1984 | Substantially Equivalent |
| K832892 | MODIFIED CHORIO-SHURE | Oct 28, 1983 | Substantially Equivalent |
| K832002 | NML-5010/5020 MULTI-DETECTOR SYSTEM | Aug 8, 1983 | Substantially Equivalent |
| K823679 | NML 6000 CT | Jan 7, 1983 | Substantially Equivalent |
| K823053 | NML-TETRA-TUBE RIA | Nov 10, 1982 | Substantially Equivalent |
| K822298 | DIAGNOSTIC RADIOIMMUNOASSAY FOR QUANTI | Sep 2, 1982 | Substantially Equivalent |
| K820523 | CHORIO-QUANT | Mar 15, 1982 | Substantially Equivalent |
| K812759 | NML CK-MB RIA | Oct 19, 1981 | Substantially Equivalent |