510(k) K791393
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 16, 1979
- Date Received
- July 11, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antigens, Histoplasma Capsulatum, All
- Device Class
- Class II
- Regulation Number
- 866.3320
- Review Panel
- MI
- Submission Type