510(k) K922047
K922047 is an FDA 510(k) premarket notification submitted by Medix Biotech, Inc. for the device "IGE ENZYME IMMUNOASSAY TEST KIT CAT.NO. KIF4064". The FDA issued a decision of Substantially Equivalent on August 5, 1992. The device falls under product code DGC (Ige, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Medix Biotech, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 5, 1992
- Date Received
- May 1, 1992
- 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