510(k) K812487
- Device
- IMMUNOGL. FRCT. OF RABBIT ANTISER.-IGM
- Applicant
- DAKO CORP.
- 510(k) number
- K812487
- Product code
- DAO
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1981-09-23
- Date received
- 1981-08-31
- Regulation
- 866.5550
- Classification name
- Igm (mu Chain Specific), Antigen, Antiserum, Control
- Medical specialty
- Immunology
- Review panel
- Immunology
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 9610099
- 9610529
- 3003423869
- 3013059683
- 3009189893
- 9610126
- 3006198300
- 3003795116
- 3019906
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code DAO #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K040431 | ROCHE DIAGNOSTICS TINA-QUANT IGM GEN.2 | Roche Diagnostics Corp. | 2004-03-10 |
| K982639 | SPIFE URINE IFE | Helena Laboratories | 1998-11-04 |
| K955908 | BOEHRINGER MANNHEIM IGM ASSAY | Boehringer Mannheim Corp. | 1996-02-09 |
| K850586 | SPQ TEST SYSTEM FOR IMMUNOGLOBULIN M | Applications Lab | 1985-03-14 |
| K841992 | MODIFICATION TO ACS CORONARY GUIDING | Advanced Cardiovascular Systems, Inc. | 1984-06-11 |
| K800450 | GEMENI IGM ASSAY | Electro-Nucleonics Laboratories, Inc. | 1980-04-24 |
| K790705 | ANTISERUM TO HUMAN IGM | Kent Laboratories, Inc. | 1979-04-12 |
Legacy Summary#
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FDA Review#
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