510(k) K990842

SAS ROTA TEST by Sa Scientific, Inc. — Product Code LIQ

K990842 is an FDA 510(k) premarket notification submitted by Sa Scientific, Inc. for the device "SAS ROTA TEST". The FDA issued a decision of Substantially Equivalent on August 9, 1999. The device falls under product code LIQ (Enzyme Linked Immunoabsorbent Assay, Rotavirus), a Class I device regulated under 21 CFR 866.3405. Sa Scientific, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 9, 1999
Date Received
March 15, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzyme Linked Immunoabsorbent Assay, Rotavirus
Device Class
Class I
Regulation Number
866.3405
Review Panel
MI
Submission Type