510(k) K010878
K010878 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "MODIFICATION TO IMMULITE HERPES I & II IGG, MODEL L2KHS2 & L2KHS6". The FDA issued a decision of Substantially Equivalent on April 18, 2001. The device falls under product code LGC (Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-Specific), a Class II device regulated under 21 CFR 866.3305. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 18, 2001
- Date Received
- March 19, 2001
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Linked Immunoabsorbent Assay, Herpes Simplex Virus, Non-Specific
- Device Class
- Class II
- Regulation Number
- 866.3305
- Review Panel
- MI
- Submission Type