ClearanceBrief
510(k) K923922 ยท HOZ Sponge, Ophthalmic

SURGICAL SPEARS

ApplicantUltracell Medical Technologies, Inc., North Stonington CT, US
DecisionSubstantially Equivalent, Mar 19, 1993
ReceivedAug 5, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923922

DateFirm and productCodeLinked 510(k)
Jan 30, 2003Ultracell Medical Technologies
Ultrakleen KSponge II Spears Catalog #: K20-5012
Terminated
HOZNone listed
Jan 30, 2003Ultracell Medical Technologies
PVA Foam Surgical Spears Catalog #: OASIS0525
Terminated
HOZNone listed
Jan 30, 2003Ultracell Medical Technologies
Lasik Spears Blunt (5) Catalog #: U/S32-100
Terminated
HOZNone listed

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