510(k) BK840004
- Device
- 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
- Applicant
- Dynatech Laboratories, Inc.
- 510(k) number
- BK840004
- Product code
- KSZ
- Decision
- Substantially Equivalent (SE)
- Decision date
- 1984-05-18
- Date received
- 1984-03-08
- Regulation
- 864.9175
- Classification name
- System, Test, Automated Blood Grouping And Antibody
- Medical specialty
- 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
- Review panel
- 510(k) Premarket Notification // Quick Links: Skip To Main Page Content Skip To Search Skip To Topics Menu Skip To Common Links U.S. Food & Drug Administration Follow FDA En Español Search FDA Home Food Drugs Medical Devices
- Clearance type
- 510(k) Traditio
- Third party reviewed
- No
Other 510(k) Records For Product Code KSZ #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K810899 | TECHNICON AUTOGROUPER 16-C SYSTEM | Technicon Instruments Corp. | 1981-05-05 |
| K790282 | ELDONCARD | Nordisk Infuser System | 1979-05-04 |
| K771098 | BLOOD GROUPING SYS., BG-9 | Technicon Instruments Corp. | 1977-08-04 |
| K770185 | RH CONTROL DILUENT | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1977-03-14 |
Legacy Summary#
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FDA Review#
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