510(k) BK040035
- Device
- Qualitative Test For HLA, Non-diagnostic
- Applicant
- Gen-Probe GTI Diagnostics
- 510(k) number
- BK040035
- Product code
- MZI
- Decision
- Substantially Equivalent (SE)
- Decision date
- 2004-07-16
- Date received
- 2004-04-19
- Regulation
- 510(k) Premarket Notification
- Classification name
- Test, Qualitative, For Hla, Non-diagnostic
- 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
Legacy Summary#
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FDA Review#
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