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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 30 Results
510(K) Number: K033186
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Product Description
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Recall
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FDA Recall
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KING LT -D Laryngeal Tube, Size 2, KLTD202, King Systems Corporation 15011 Herriman Boulevard, Nob... 2 01/27/2011 King Systems Corp.
Cardiac ResQ Kit, Size 5, CRQ425, King Systems Corporation 15011 Herriman Boulevard, Noblesville, I... 2 01/27/2011 King Systems Corp.
Cardiac ResQ Kit, Size 4, CRQ424, King Systems Corporation 15011 Herriman Boulevard, Noblesville, I... 2 01/27/2011 King Systems Corp.
KING LT -D Size 3, 10-0002, Oropharyngeal Airway. King Systems Corporation 15011 Herriman Boulevard... 2 01/27/2011 King Systems Corp.
KING LTS -D, Size 5, 10-0027, Oropharyngeal Airway. King Systems Corporation 15011 Herriman Bouleva... 2 01/27/2011 King Systems Corp.
KING LTS -D, Size 4, 10-0026, Oropharyngeal Airway. King Systems Corporation 15011 Herriman Bouleva... 2 01/27/2011 King Systems Corp.
KING LTS -D, Size 3, 10-0025, Oropharyngeal Airway. King Systems Corporation, 15011 Herriman Boul... 2 01/27/2011 King Systems Corp.
KING LT-D Size 5, 10-0004, Oropharyngeal Airway. King Systems Corporation 15011 Herriman Boulevard, ... 2 01/27/2011 King Systems Corp.
KING LT -D Size 4, 10-0003, Oropharyngeal Airway. King Systems Corporation 15011 Herriman Boulevard... 2 01/27/2011 King Systems Corp.
Cardiac ResQ Kit , Size 3, CRQ423, Oropharyngeal Airway. King Systems Corporation 15011 Herriman Bou... 2 01/27/2011 King Systems Corp.
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