510(k) K883558
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