510(k) K020603
K020603 is an FDA 510(k) premarket notification submitted by Good Biotech Corp. for the device "CRPEX-HS C-REACTIVE PROTEIN LIT ASSAY, CATALOG NO. 1010". The FDA issued a decision of Substantially Equivalent on June 13, 2002. The device falls under product code DCN (System, Test, C-Reactive Protein), a Class II device regulated under 21 CFR 866.5270. Good Biotech Corp. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 13, 2002
- Date Received
- February 25, 2002
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Test, C-Reactive Protein
- Device Class
- Class II
- Regulation Number
- 866.5270
- Review Panel
- IM
- Submission Type