510(k) K802337
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 31, 1980
- Date Received
- September 26, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antisera, All Types, Streptococcus Pneumoniae
- Device Class
- Class I
- Regulation Number
- 866.3740
- Review Panel
- MI
- Submission Type