510(k) K033864
K033864 is an FDA 510(k) premarket notification submitted by Genzyme Corp. for the device "GENZYME OSOM TRICHOMONAS RAPID TEST". The FDA issued a decision of Substantially Equivalent on April 2, 2004. The device falls under product code JWZ (Kit, Screening, Trichomonas), a Class I device regulated under 21 CFR 866.2660. Genzyme Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 2, 2004
- Date Received
- December 12, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Screening, Trichomonas
- Device Class
- Class I
- Regulation Number
- 866.2660
- Review Panel
- MI
- Submission Type