510(k) K864802
K864802 is an FDA 510(k) premarket notification submitted by Coulter Electronics, Inc. for the device "DART DIGOXIN ASSAY". The FDA issued a decision of Substantially Equivalent on February 12, 1987. The device falls under product code LCS (Radioimmunoassay, Digoxin (125-I)), a Class II device regulated under 21 CFR 862.3320. Coulter Electronics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 12, 1987
- Date Received
- December 9, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Digoxin (125-I)
- Device Class
- Class II
- Regulation Number
- 862.3320
- Review Panel
- TX
- Submission Type