510(k) K862067
K862067 is an FDA 510(k) premarket notification submitted by American Dade for the device "STRATUS DIGITOXIN FLUOROMETRIC ENZYME IMMUNOASSAY". The FDA issued a decision of Substantially Equivalent on June 16, 1986. The device falls under product code LFM (Enzyme Immunoassay, Digitoxin), a Class II device regulated under 21 CFR 862.3300. American Dade has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 16, 1986
- Date Received
- May 30, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Immunoassay, Digitoxin
- Device Class
- Class II
- Regulation Number
- 862.3300
- Review Panel
- TX
- Submission Type