510(k) K864142
K864142 is an FDA 510(k) premarket notification submitted by United Biotech, Inc. for the device "UBI MAGIWEL(TM) IGE QUANTITATIVE AND QUALITATIVE". The FDA issued a decision of Substantially Equivalent on December 3, 1986. The device falls under product code DGC (Ige, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. United Biotech, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 3, 1986
- Date Received
- October 22, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ige, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5510
- Review Panel
- IM
- Submission Type