FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
HDL PRECIPITANT REAGENT SET
K Number: K821203
·
Decision Jul 13, 1982
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
65
Applicant Total
21
Review Days
77
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Basic Information
- Device Name
- HDL PRECIPITANT REAGENT SET
- K Number
- K821203
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1475
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Omega Medical Electronics
- Date Received
- April 27, 1982
- Decision Date
- July 13, 1982
- Product Code
- LBR
- 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 |
|---|---|---|---|
| LBR | Ldl & Vldl Precipitation, Hdl | FDA class 1 | Clinical Chemistry |
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Other Clearances by Omega Medical Electronics
| K Number | Device Name | ||
|---|---|---|---|
| K823691 | PHOSPHORUS REAGENT SET | Jan 7, 1983 | Substantially Equivalent |
| K821204 | GLUCOSE(ENZYMATIC) REAGENT SET | Jul 22, 1982 | Substantially Equivalent |
| K821206 | SGPT-UV REAGENT SET | Jul 22, 1982 | Substantially Equivalent |
| K821212 | UREA NITROGEN REAGENT SET | Jul 22, 1982 | Substantially Equivalent |
| K821201 | LDH-UV REAGENT SET | Jul 20, 1982 | Substantially Equivalent |
| K821205 | TRIGLYCERIDE REAGENT SET | Jul 20, 1982 | Substantially Equivalent |
| K821208 | SGOT-UV REAGENT SET | Jul 20, 1982 | Substantially Equivalent |
| K821207 | SGPT REAGENT SET | Jul 14, 1982 | Substantially Equivalent |
| K821209 | SGOT REAGENT SET | Jul 14, 1982 | Substantially Equivalent |
| K821199 | CREATININE REAGENT SET | Jul 13, 1982 | Substantially Equivalent |