510(k) K962719
K962719 is an FDA 510(k) premarket notification submitted by Hycor Biomedical, Inc. for the device "HYCOR HY.TEC/MANUAL SS-A AUTO-ANTIBODY". The FDA issued a decision of Substantially Equivalent on March 7, 1997. The device falls under product code LLL (Extractable Antinuclear 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 7, 1997
- Date Received
- July 1, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Extractable Antinuclear Antibody, Antigen And Control
- Device Class
- Class II
- Regulation Number
- 866.5100
- Review Panel
- IM
- Submission Type