ClearanceBrief
510(k) K830014 ยท CAK Microfilter, Blood Transfusion

HEMA - NV TRANS. BLOOD FILTER 100/800

ApplicantAbbott Laboratories, Abbott Park IL, US
DecisionSubstantially Equivalent, Jan 17, 1983
ReceivedJan 3, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830014

DateFirm and productCodeLinked 510(k)
Feb 27, 2007Hospira Inc.
LifeShield Latex-Free Primary I.V. Pump Set with Distal Microbore Patient Line and Gravity Flow Prevention Valve, Convertible Pin, 110 Inch with High-Pressure Filter, Orange Polyethylene-Lined/Light R
Terminated
FPANone listed
Feb 8, 2006Hospira Inc.
Hospira Latex Free Blood Secondary Set, 26 inch with Secure Lock; Made in Costa Rica, Hospira, Inc., Lake Forest, IL 60045 U.S.A.
Terminated
FPANone listed
Nov 24, 2005Hospira Inc.
LifeShield Latex-Free HEMA Blood PlumSet, Nonvented, 110 Inch with 210 Micron Filter, Prepierced Injection Site and OPTION-LOK, Dual Channel, Capped Secondary Port; a sterile Rx blood administration s
Terminated
BRZNone listed
Nov 15, 2005Hospira Inc.
LifeShield Latex-Free HEMA Blood PlumSet; Nonvented, 100 inch, with 210 Micron Filter, Prepierced Injection Site and Option-Lok, Dual Channel Capped Secondary Port; Hospira, Inc., Lake Forest, IL 6004
Terminated
BRZNone listed
Nov 15, 2005Hospira Inc.
LifeShield Latex-Free HEMA Y-Type Blood PlumSet, Nonvented, 122 inch, with 210 Micron Filter, Prepierced Injection Site, Prepierced Secondary Port and Option-Lok for use with Plum Series Infusers; Hos
Terminated
BRZNone listed
Nov 15, 2005Hospira Inc.
LifeShield Latex-Free HEMA Y-Type Blood PlumSet, Nonvented, 122 inch, with 210 Micron Filter, Inline Dual Channel Cassette, 2 Clave Ports and Option-Lok for use with Plum Series Infusers; Hospira, Inc
Terminated
BRZNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.