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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 24 Results
510(K) Number: K091980
 
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Product Description
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FDA Recall
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ACL TOP (Base) PN 000280000 Bench top, fully automated, random access analyzer designed specifical... 2 10/25/2010 Instrumentation Laboratory Co.
ACL TOP CTS PN 000280020 Bench top, fully automated, random access analyzer designed specifically... 2 10/25/2010 Instrumentation Laboratory Co.
ACL TOP 700 LAS PN 000280030 Bench top, fully automated, random access analyzer designed specific... 2 10/25/2010 Instrumentation Laboratory Co.
ACL TOP 500 CTS PN 000280040 Bench top, fully automated, random access analyzer designed specific... 2 10/25/2010 Instrumentation Laboratory Co.
Instrumentation Laboratory ACL TOP 500 CTS PN 0000280040 ACL TOP is a bench top, fully automat... 2 09/14/2012 Instrumentation Laboratory Co.
Instrumentation Laboratory ACL TOP 700 LAS PN 0000280030 ACL TOP is a bench top, fully automat... 2 09/14/2012 Instrumentation Laboratory Co.
Instrumentation Laboratory ACL TOP CTS PN 0000280020 ACL TOP is a bench top, fully automated, r... 2 09/14/2012 Instrumentation Laboratory Co.
Instrumentation Laboratory ACL TOP 700 PN 0000280010 ACL TOP is a bench top, fully automated, ra... 2 09/14/2012 Instrumentation Laboratory Co.
Instrumentation Laboratory ACL TOP 700 CTS PN 0000280050 ACL TOP is a bench top, fully automat... 2 09/14/2012 Instrumentation Laboratory Co.
Instrumentation Laboratory ACL TOP (Base) PN 0000280000 ACL TOP is a bench top, fully automated,... 2 09/14/2012 Instrumentation Laboratory Co.
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