510(k) K880574
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 4, 1988
- Date Received
- February 10, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Susceptibility Test Powders, Antimicrobial
- Device Class
- Class II
- Regulation Number
- 866.1640
- Review Panel
- MI
- Submission Type