510(k) K082329
K082329 is an FDA 510(k) premarket notification submitted by Viramed Biotech AG for the device "VIRAMED BIOTECH AG BORRELIA B31 IGM VIRASTRIPE". The FDA issued a decision of Substantially Equivalent on August 5, 2009. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. Viramed Biotech AG has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 5, 2009
- Date Received
- August 14, 2008
- 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