510(k) K932603
- Device
- APOLIPOPROTIEN B (APO B)
- Applicant
- SIGMA DIAGNOSTICS, INC.
- 510(k) number
- K932603
- Product code
- JHN
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1994-06-02
- Date received
- 1993-05-28
- Regulation
- 862.1475
- Classification name
- Turbidimetric Method, Lipoproteins
- Medical specialty
- Clinical Chemistry
- Review panel
- Clinical Chemistry
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Statement
- Third party reviewed
- No
Applicant Contact#
- Contact
- WILLIAM R GILBERT
- Address
- 545 S. Ewing Ave. St. Louis MO US 63103 63103
FDA Registration Numbers#
- 9610126
- 3006198300
- 3004493545
- 8040374
- 3008517993
- 3003795116
- 9680746
- 2432235
- 9610529
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code JHN #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K950382 | APOLIPOPROTEIN B IMMUNOTURBIDIEMETRIC KIT | Randox Laboratories, Ltd. | 1995-09-15 |
| K950383 | APOLIPOPROTEIN A-I IMMUNOTURBIDIMETRIC KIT | Randox Laboratories, Ltd. | 1995-09-15 |
| K952615 | WAKO AUTOKIT APO A1 | Wako Chemicals USA, Inc. | 1995-09-08 |
| K952425 | OLYMPUS APOLIPOPROTEIN A1 IMMUNOTURBIDIMETRIC REAGENT | Olympus America, Inc. | 1995-07-05 |
| K952466 | OLYMPUS APOLIPOPROTEIN B IMMUNOTURBIDIMETRIC REAGENT | Olympus America, Inc. | 1995-06-05 |
| K932606 | APOLIPOPROTIEN A-1 (APO A-1) | Sigma Diagnostics, Inc. | 1994-06-02 |
Legacy Summary#
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FDA Review#
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