510(k) K911627
K911627 is an FDA 510(k) premarket notification submitted by General Biometrics, Inc. for the device "IMMUNODOT BORRELIA (LYME) TEST". The FDA issued a decision of Substantially Equivalent on April 8, 1992. The device falls under product code LSR (Reagent, Borrelia Serological Reagent), a Class II device regulated under 21 CFR 866.3830. General Biometrics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 8, 1992
- Date Received
- April 11, 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