510(k) K883558

VITEK GRAM-NEGATIVE IDENTIFICATION CARD by Vitek Systems, Inc. — Product Code JSS

K883558 is an FDA 510(k) premarket notification submitted by Vitek Systems, Inc. for the device "VITEK GRAM-NEGATIVE IDENTIFICATION CARD". The FDA issued a decision of Substantially Equivalent on September 16, 1988. The device falls under product code JSS (Kit, Identification, Enterobacteriaceae), a Class I device regulated under 21 CFR 866.2660. Vitek Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 16, 1988
Date Received
August 19, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Kit, Identification, Enterobacteriaceae
Device Class
Class I
Regulation Number
866.2660
Review Panel
MI
Submission Type