510(k) K021395

MODIFICATION TO 30 EXTENSION SET by Churchill Medical Systems, Inc. — Product Code FPA

K021395 is an FDA 510(k) premarket notification submitted by Churchill Medical Systems, Inc. for the device "MODIFICATION TO 30 EXTENSION SET". The FDA issued a decision of Substantially Equivalent on May 13, 2002. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Churchill Medical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 13, 2002
Date Received
May 2, 2002
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Administration, Intravascular
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type