510(k) K790776
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 23, 1979
- Date Received
- April 20, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Media, Potentiating For In Vitro Diagnostic Use
- Device Class
- Class II
- Regulation Number
- 864.9600
- Review Panel
- HE
- Submission Type