510(k) K935417
K935417 is an FDA 510(k) premarket notification submitted by David A. Fuccillo, Ph.D. for the device "JO-1 EIA TEST KIT". The FDA issued a decision of Substantially Equivalent on May 5, 1994. The device falls under product code LLL (Extractable Antinuclear Antibody, Antigen And Control), a Class II device regulated under 21 CFR 866.5100. David A. Fuccillo, Ph.D. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 5, 1994
- Date Received
- November 9, 1993
- 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