510(k) K800205

RIA PHASE DIGOXIN by Boehringer Mannheim Corp. — Product Code DPO

K800205 is an FDA 510(k) premarket notification submitted by Boehringer Mannheim Corp. for the device "RIA PHASE DIGOXIN". The FDA issued a decision of Substantially Equivalent on March 19, 1980. The device falls under product code DPO (Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Coated Tube Sep.), a Class II device regulated under 21 CFR 862.3320. Boehringer Mannheim Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 19, 1980
Date Received
January 30, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Radioimmunoassay, Digoxin (125-I), Rabbit Antibody, Coated Tube Sep.
Device Class
Class II
Regulation Number
862.3320
Review Panel
TX
Submission Type