Intertherapy, Inc.

FDA Regulatory Profile

Intertherapy, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 20, 1991.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K913763INTERPRET(TM) CATHETER LINEAR TRANSLATORNovember 20, 1991
K912600INTERPRET(TM) INTRAVASCULAR IMAGING CATHETERNovember 19, 1991
K910281INTRAVASCULAR IMAGING SYSTEM/MODIFIEDMay 13, 1991
K900305INTRAVASCULAR IMAGING SYSTEMSApril 20, 1990
K895159INTRAVASCULAR IMAGING SYSTEMMarch 12, 1990