510(k) K802339
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 18, 1980
- Date Received
- September 26, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antigen, Ha (Including Ha Control), Rubella
- Device Class
- Class II
- Regulation Number
- 866.3510
- Review Panel
- MI
- Submission Type