510(k) K770322

PHALDEBAS DIGOXIN RIA by Pharmacia, Inc. — Product Code LCS

K770322 is an FDA 510(k) premarket notification submitted by Pharmacia, Inc. for the device "PHALDEBAS DIGOXIN RIA". The FDA issued a decision of Substantially Equivalent on April 5, 1977. The device falls under product code LCS (Radioimmunoassay, Digoxin (125-I)), a Class II device regulated under 21 CFR 862.3320. Pharmacia, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 5, 1977
Date Received
February 17, 1977
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