510(k) K910666
K910666 is an FDA 510(k) premarket notification submitted by Vitek Systems, Inc. for the device "VITEK ANAEROBE IDENTIFICATION CARD, MODIFICATION". The FDA issued a decision of Substantially Equivalent on April 3, 1991. The device falls under product code JSP (Kit, Anaerobic Identification), 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
- April 3, 1991
- Date Received
- February 11, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Anaerobic Identification
- Device Class
- Class I
- Regulation Number
- 866.2660
- Review Panel
- MI
- Submission Type