510(k) K871732

CHURCHILL-H VENTED IV SET W/METERING CHAMBERS by Churchill Corp. — Product Code FPA

K871732 is an FDA 510(k) premarket notification submitted by Churchill Corp. for the device "CHURCHILL-H VENTED IV SET W/METERING CHAMBERS". The FDA issued a decision of Substantially Equivalent on June 15, 1987. The device falls under product code FPA (Set, Administration, Intravascular), a Class II device regulated under 21 CFR 880.5440. Churchill Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 15, 1987
Date Received
May 5, 1987
Clearance Type
Traditional
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