FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

.22 & 1.2 MICRON IV FILTERS

K Number: K894954 · Decision Nov 13, 1989
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
97
Applicant Total
12
Review Days
101

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Basic Information

Device Name
.22 & 1.2 MICRON IV FILTERS
K Number
K894954
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Churchill Medical Systems, Inc.
Date Received
August 4, 1989
Decision Date
November 13, 1989
Product Code
FPB
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FPB Filter, Infusion Line

Similar 510(k) Clearances

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Other Clearances by Churchill Medical Systems, Inc.

K Number Device Name
K041038 CHURCHILL MEDICAL DUAL CHAMBER EMPTY CONTAINER
K021395 MODIFICATION TO 30 EXTENSION SET
K013949 UNIVERSAL VIAL ACCESS SPIKE WITH NEEDLELESS CONNECTOR
K020544 WING SAFE INFUSION SET 20 GA, SHS2000 SERIES; WING SAFE INFUSION SET 19 GA, SHS1900 SERIES; WING SAFE INFUSION SET 22 GA
K013950 VENTED VIAL ACCESS DEVICE
K012157 CHURCHILL MEDICAL SYSTEMS STOPCOCK
K011888 PRESSURE ACTIVATED CHECK VALVE
K011336 PRIMARY SOLUTION SET WITH UNIVERSAL SPIKE, INJECTION SITE AND MALE LUER LOCK
K896333 CMS IV FILTERS
K884370 CMS IV EXTENSION SETS
Search all 12 clearances from Churchill Medical Systems, Inc. →