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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K923922
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FDA Recall
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Ultrakleen KSponge II Spears Catalog #: K20-5012 2 01/30/2003 Ultracell Medical Technologies
Lasik Spears Blunt (5) Catalog #: U/S32-100 2 01/30/2003 Ultracell Medical Technologies
PVA Foam Surgical Spears Catalog #: OASIS0525 2 01/30/2003 Ultracell Medical Technologies
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