510(k) K952243

EXTENSION SET/I.V. SET by Coast Medical, Inc. — Product Code FPK

K952243 is an FDA 510(k) premarket notification submitted by Coast Medical, Inc. for the device "EXTENSION SET/I.V. SET". The FDA issued a decision of Substantially Equivalent on July 26, 1995. The device falls under product code FPK (Tubing, Fluid Delivery), a Class II device regulated under 21 CFR 880.5440. Coast Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 26, 1995
Date Received
May 12, 1995
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