510(k) K884370

CMS IV EXTENSION SETS by Churchill Medical Systems, Inc. — Product Code FPK

K884370 is an FDA 510(k) premarket notification submitted by Churchill Medical Systems, Inc. for the device "CMS IV EXTENSION SETS". The FDA issued a decision of Substantially Equivalent on November 7, 1988. The device falls under product code FPK (Tubing, Fluid Delivery), 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
November 7, 1988
Date Received
October 18, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tubing, Fluid Delivery
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type