510(k) K990842
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