510(k) K960147

SAS SALMONELLA 0 GROUP E FACTORS 1,3,10,15,19,34 ANTISERUM by Sa Scientific, Inc. — Product Code GRM

K960147 is an FDA 510(k) premarket notification submitted by Sa Scientific, Inc. for the device "SAS SALMONELLA 0 GROUP E FACTORS 1,3,10,15,19,34 ANTISERUM". The FDA issued a decision of Substantially Equivalent on March 12, 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
March 12, 1996
Date Received
January 11, 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