510(k) K961964
K961964 is an FDA 510(k) premarket notification submitted by Sa Scientific, Inc. for the device "SAS SALMONELLA O GROUP H FACTORS 14,24,25 ANTISERUM". The FDA issued a decision of Substantially Equivalent on June 18, 1996. The device falls under product code GRM (Antisera, All Groups, Salmonella Spp.), a Class II device regulated under 21 CFR 866.3550. Sa Scientific, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 18, 1996
- Date Received
- May 20, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antisera, All Groups, Salmonella Spp.
- Device Class
- Class II
- Regulation Number
- 866.3550
- Review Panel
- MI
- Submission Type