510(k) K890774
K890774 is an FDA 510(k) premarket notification submitted by Antibodies, Inc. for the device "GIARDEIA(TM)". The FDA issued a decision of Substantially Equivalent on April 4, 1989. The device falls under product code KHW (Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.), a Class II device regulated under 21 CFR 866.3220. Antibodies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 4, 1989
- Date Received
- February 15, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.
- Device Class
- Class II
- Regulation Number
- 866.3220
- Review Panel
- MI
- Submission Type