510(k) K872634

CUTTER PUREFLO PLUS IV FILTER by Miles Laboratories, Inc. — Product Code FPB

K872634 is an FDA 510(k) premarket notification submitted by Miles Laboratories, Inc. for the device "CUTTER PUREFLO PLUS IV FILTER". The FDA issued a decision of Substantially Equivalent on August 4, 1987. The device falls under product code FPB (Filter, Infusion Line), a Class II device regulated under 21 CFR 880.5440. Miles Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 4, 1987
Date Received
July 6, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Infusion Line
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type