510(k) K262156
K262156 is an FDA 510(k) premarket notification submitted by Abbott Laboratories for the device "Anti-HCV Next". The FDA issued a decision of Substantially Equivalent on Sep 23, 2026. The device falls under product code MZO (Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus), a Class II device regulated under 21 CFR 866.3169. Abbott Laboratories has 889 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 23, 2026
- Date Received
- Jun 26, 2026
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus
- Device Class
- Class II
- Regulation Number
- 866.3169
- Review Panel
- MI
- Submission Type
- 510(k)