510(k) K040241
K040241 is an FDA 510(k) premarket notification submitted by Genzyme Corp. for the device "N-GENEOUS WIDE RANGE CRP REAGENT AND CALIBRATOR SET". The FDA issued a decision of Substantially Equivalent on June 25, 2004. The device falls under product code DCK (C-Reactive Protein, Antigen, Antiserum, And Control), a Class II device regulated under 21 CFR 866.5270. Genzyme Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 25, 2004
- Date Received
- February 3, 2004
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- C-Reactive Protein, Antigen, Antiserum, And Control
- Device Class
- Class II
- Regulation Number
- 866.5270
- Review Panel
- IM
- Submission Type