510(k) K884017

ROTACUBE by Difco Laboratories, Inc. — Product Code LIQ

K884017 is an FDA 510(k) premarket notification submitted by Difco Laboratories, Inc. for the device "ROTACUBE". The FDA issued a decision of Substantially Equivalent on January 24, 1989. The device falls under product code LIQ (Enzyme Linked Immunoabsorbent Assay, Rotavirus), a Class I device regulated under 21 CFR 866.3405. Difco Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 1989
Date Received
September 22, 1988
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