510(k) K955361
K955361 is an FDA 510(k) premarket notification submitted by Incstar Corp. for the device "INCSTAR CYTOMEGALOVIRUS IGG ELISA ASSAY". The FDA issued a decision of Substantially Equivalent on July 22, 1996. The device falls under product code LFZ (Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. Incstar Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 22, 1996
- Date Received
- November 22, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus
- Device Class
- Class II
- Regulation Number
- 866.3175
- Review Panel
- MI
- Submission Type