ClearanceBrief
510(k) K033941 ยท HQF Laser, Ophthalmic

MILLENNIUM MICROSURGICAL SYSTEM AND PERISTALTIC PHACO PACK

ApplicantBausch & Lomb, Inc., St. Louis MO, US
DecisionSubstantially Equivalent, Feb 10, 2004
ReceivedDec 19, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033941

DateFirm and productCodeLinked 510(k)
May 28, 2010Bausch & Lomb Inc
Bausch & Lomb Millennium Advanced Flow System Phaco Pack, Model CX5310, 6 packs/box, RX, Sterile. The firm name on the label is Bausch & Lomb Incorporated, Rochester, NY. The plastic needle wrench c
Terminated
HQFNone listed

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