510(k) K910230
K910230 is an FDA 510(k) premarket notification submitted by Vitek Systems, Inc. for the device "LYME-SPOT IF KIT". The FDA issued a decision of Substantially Equivalent on August 30, 1991. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. Vitek Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 30, 1991
- Date Received
- January 18, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Reagent, Borrelia Serological Reagent
- Device Class
- Class II
- Regulation Number
- 866.3830
- Review Panel
- MI
- Submission Type