510(k) K954896
K954896 is an FDA 510(k) premarket notification submitted by Hycor Biomedical, Inc. for the device "HYTEC AUTOIMMUNE KITS (SM)". The FDA issued a decision of Substantially Equivalent on March 22, 1996. The device falls under product code LKP (Anti-Sm Antibody, Antigen And Control), a Class II device regulated under 21 CFR 866.5100. Hycor Biomedical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 22, 1996
- Date Received
- September 19, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Anti-Sm Antibody, Antigen And Control
- Device Class
- Class II
- Regulation Number
- 866.5100
- Review Panel
- IM
- Submission Type