Atlas FDA

ARTERIA BLOOD FILTER

FDA 510(k) clearance K021293 · decided 2002-08-22

Clearance details

K-number
K021293
Device name
ARTERIA BLOOD FILTER
Applicant
Arteria Medical Science, Inc.
Decision
Substantially Equivalent
Date received
2002-04-23
Decision date
2002-08-22
Days to decision
121 days
Clearance type
Traditional
Product code
FPB
Device class
2
Regulation number
880.5440
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Newburyport, MA, US
Third-party review
No
Expedited review
No

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PALL LEA FILTER (LIPID EMULSION FILTER) (I.V. FILTER) (K954331)Pall Biomedical Products Co.1997-01-09
I.V. FILTER SET (K933523)Mediziv Medical Products 1987 , Ltd.1995-05-19
40 MICRON BLOOD TRANSFUSION FILTER (K941628)Douglas Medical Products Corp.1995-02-16
1.2 MICRON AIR ELIMINATING FILTER (K942625)The Medi-Dose Group1994-10-07
PHARMASSURE LARGE VOLUME TRANSFER FILTERS (K943127)Gelman Sciences, Inc.1994-09-29
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Recalls involving this device

No recalls on record reference this clearance.