ClearanceBrief
510(k) K040266 ยท KNW Instrument, Biopsy

CORE NEEDLE BIOPSY

ApplicantRemington Medical, Inc., Alpharetta GA, US
DecisionSubstantially Equivalent, Jul 9, 2004
ReceivedFeb 5, 2004
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K040266

DateFirm and productCodeLinked 510(k)
Mar 7, 2011Remington Medical Inc.
Automatic Cutting Needle, Soft Tissue Biopsy Needle, NAC-14010MLL, 14ga (2.1mm) x 10cm (10), Remington Medical, Inc.
Terminated
KNWNone listed
Mar 7, 2011Remington Medical Inc.
Automatic Cutting Needle, Soft Tissue Biopsy Needle, NAC-1820MLL, 18ga (1.3mm) x 20cm (10), Remington Medical, Inc.
Terminated
KNWNone listed
Mar 7, 2011Remington Medical Inc.
Automatic Cutting Needle, Soft Tissue Biopsy Needle, NAC-1825MLL, 18ga (1.3mm) x 25cm (10), Remington Medical, Inc.
Terminated
KNWNone listed
Mar 7, 2011Remington Medical Inc.
Automatic Cutting Needle, Soft Tissue Biopsy Needle, NAC-1820M, 18ga (1.3mm) x 20cm (10), Remington Medical, Inc.
Terminated
KNWNone listed
Mar 7, 2011Remington Medical Inc.
Automatic Cutting Needle, Soft Tissue Biopsy Needle, NAC-1825M, 18ga (1.3mm) x 25cm (10), Remington Medical, Inc.
Terminated
KNWNone listed

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